Inhibition of cancer metastasis

ABSTRACT

P-Selectin on platelets and endothelium binds cell surface chondroitin sulfate (CS) proteoglycans, which are abundantly and stably expressed on the surface many cancer cells. Binding of the cancer cells through the CS moieties may be blocked to inhibit the interaction of cancer cells with platelets and endothelium. The present inventors disclose compositions and methods for the inhibition of cancer metastasis.

CROSS-REFERENCES TO RELATED APPLICATIONS

This application claims the benefit and priority as a divisionalapplication under 35 U.S.C. 121 of U.S. utility patent application Ser.No. 12/286,950, filed Oct. 4, 2008, now U.S. Pat. No. 8,173,103, whichclaims benefit and priority as a continuation-in-part application ofU.S. Utility patent application Ser. No. 11/694,370, filed Mar. 30,2007, now abandoned, which claims priority from U.S. Provisionalapplication No. 60/788,018 filed on Mar. 31, 2006, the contents of allof which applications are incorporated herein by reference in theirentirety.

STATEMENT REGARDING FEDERALLY SPONSORED RESEARCH

This invention was made with government support under grantDAMD17-0101-0366 awarded by the Department of Defense and grant CA089480awarded by the National Institutes of Health. The government has certainrights in the invention.

BACKGROUND OF THE INVENTION

Cancer metastasis is strongly correlated with a poor prognosis ofpatients. The multi-step process of metastasis includes release ofmalignant cells from the primary neoplasm, migration of cancer cellsinto circulation, adhesion at distant sites, and growth of thedisseminated cancer cells within the vessels or within the tissuefollowing extravasation. Each step in this process requires differenttypes of interaction between cancer cells and the host microenvironment.

The selectin family of adhesion molecules include P-Selectin,L-Selectin, and E-Selectin. P-Selectin is a 140 kDa protein that iscommonly expressed on the surface of a variety of cell types, including,but not limited to, platelets and endothelium. (See, for example,GenBank Accession No. P16109 (Homo sapiens) or GenBank Accession No.AAA40008 (Mus musculus).) E-Selectin is commonly expressed in a varietyof cell types, including, for example, vascular endothelium. (See, forexample, NP_000441 (Homo sapiens) or AAA37577 (Mus musculus).)L-selectin is expressed on lymphocytes.

Cell surface proteoglycans (PGs) are another class of cell surfaceadhesion molecules. These PGs may comprise glycosaminoglycan (GAG) sidechains covalently bound to a protein core. The GAG side chain can beheparin sulfate (HS) or chondroitin sulfate (CS).

The mammary cell line 4T1 is a model system of spontaneous breast cancermetastasis. This model exhibits a deficiency in the oligosaccharidessialyl Lewis X (sLe^(x)) and sialyl Lewis A (sLe^(a)). This deficiencyresults in diminished homotypic adhesion and higher motility of thetumor cells.

BRIEF SUMMARY OF THE INVENTION

The present inventors demonstrate that P-Selectin binds to chondroitinsulfate proteoglycans on the surface of cancer cells. Additionally, thepresent inventors demonstrate that platelets which express P-Selectinbind to chondroitin sulfate proteoglycans on the surface of cancer cellsthrough the P-Selectin molecule. The inventors further demonstrate thatendothelial cells which express P-Selectin bind to chondroitin sulfateproteoglycans on the surface of cancer cells through the P-Selectinmolecule. More importantly, the inventors demonstrate that inhibition ofthe aforementioned P-Selectin binding to chondroitin sulfateproteoglycans prevents metastasis by preventing tumor cell interactionwith platelets or tumor cell interaction with endothelial cells atsecondary sites. Inhibition of the interaction of tumor cell chondroitinsulfate proteoglycans with platelets or endothelium may be achieved inmultiple ways as set forth herein.

In certain embodiments of the present invention, compositions aredisclosed for the inhibition of cancer metastasis. In particularembodiments, such a composition for inhibiting metastasis of a cancercell may comprise a chondroitin sulfate ligand. In further embodiments,such a composition for inhibiting metastasis of a cancer cell maycomprise a P-Selectin ligand. In yet further embodiments, such acomposition for inhibiting metastasis of a cancer cell may comprise aninhibitor of synthesis of chondroitin sulfate or sulfation ofchondroitin sulfate.

In various embodiments of the present invention, methods of inhibitingmetastasis are disclosed. In one embodiment, a method of inhibitingmetastasis comprises blocking the interaction of a first cell comprisingchondroitin sulfate with a second cell by contacting said first cellwith a chondroitin sulfate ligand.

In another embodiment of the present invention, a method of inhibitingmetastasis may comprise blocking the interaction of a first cellcomprising chondroitin sulfate with a second cell comprising P-Selectinby contacting said second cell with a P-Selectin ligand.

In particular embodiments of the present invention, a method ofinhibiting metastasis may comprise contacting a cancer cell with achondroitin sulfate synthesis inhibitor or a chondroitin sulfatesulfation inhibitor.

Another embodiment of the invention provides a method of identifying acandidate drug to treat cancer comprising: testing one or more compoundsfor inhibiting a chondroitin sulfate synthesis enzyme to identify acompound that inhibits a chondroitin sulfate synthesis enzyme; wherein acompound that inhibits a chondroitin sulfate synthesis enzyme is acandidate drug to treat cancer.

Another embodiment of the invention provides a method of identifying acandidate drug to inhibit metastasis comprising: (a) testing one or morecompounds for binding to Melanoma Chondroitin Sulfate Proteoglycan,Syndecan-1, Syndecan-4, or Neuropilin-1 to identify a compound thatbinds to Melanoma Chondroitin Sulfate Proteoglycan, Syndecan-1,Syndecan-4, or Neuropilin-1; wherein a compound that binds to MelanomaChondroitin Sulfate Proteoglycan, Syndecan-1, Syndecan-4, orNeuropilin-1 is a candidate drug to treat cancer.

Another embodiment of the invention provides a method of inhibitingmetastasis in a mammal afflicted with cancer or suspected to beafflicted with cancer comprising: (a) administering to the mammal anantibody against, or T cells that specifically recognize, MelanomaChondroitin Sulfate Proteoglycan (MCSP), Syndecan-1, Syndecan-4, orNeuropilin-1; or (b) vaccinating the mammal with MCSP, Syndecan-1,Syndecan-4, Neuropilin-1, or a peptide thereof.

Another embodiment of the invention provides a method of screening foran agent to inhibit cancer metastasis comprising: testing one or morecompounds not previously known to treat cancer for effect on methylationof DNA to identify an agent that causes hypermethylation of DNA; testingthe agent for inhibition of cancer metastasis in vivo in a mammal.

Another embodiment provides a method of treating breast cancercomprising: (a) administering to a patient an antibody against, or Tcells that specifically recognize, Melanoma Chondroitin SulfateProteoglycan; or (b) vaccinating a patient with Melanoma ChondroitinSulfate Proteoglycan or a peptide thereof.

Another embodiment provides a method of inhibiting metastasis in amammal afflicted with cancer or suspected to be afflicted with cancercomprising: (a) administering to the mammal an antibody against, or Tcells that specifically recognize, Syndecan-4; or (b) vaccinating themammal with Syndecan-4 or a peptide thereof.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 illustrates flow cytometry analysis of anti-sialyl Lewis Xmonoclonal antibody (FH6, KM93, or CSLEX) binding to 4T1 cellstransfected with either vector alone (4T1-EGFP) or transfected withvector containing a DNA insert which expresses fucosyltransferase III(4T1-FTIII). FIG. 1A illustrates analysis of 4T1-EGFP, cells incubatedwith fluorescein isothiocyanate (FITC) conjugated secondary antibody.FIG. 1B illustrates analysis of 4T1-FTIII cells incubated withFITC-conjugated secondary antibody. FIG. 1C illustrates analysis of4T1-EGFP cells incubated with FH6 primary antibody followed byFITC-conjugated secondary antibody. FIG. 1D illustrates analysis of4T1-FTIII cells incubated with FH6 primary antibody followed byFITC-conjugated secondary antibody. FIG. 1E illustrates analysis of4T1-EGFP cells incubated with KM93 primary antibody followed byFITC-conjugated secondary antibody. FIG. 1F illustrates analysis of4T1-FTIII cells incubated with KM93 primary antibody followed byFITC-conjugated secondary antibody. FIG. 1G illustrates analysis of4T1-EGFP cells incubated with CSLEX1 primary antibody followed byFITC-conjugated secondary antibody. FIG. 1H illustrates analysis of4T1-FTIII cells incubated with CSLEX1 primary antibody followed byFITC-conjugated secondary antibody.

FIG. 2 illustrates E-Selectin and P-Selectin binding to 4T1 cells.Either 4T1-EGFP or 4T1-FTIII cells were first incubated with humanIgG-chimeric E-Selectin or human IgG-chimeric P-Selectin and thenstained with FITC-conjugated goat anti-human IgG. 4T1-EGFP cells areillustrated by dashed line histograms and 4T1-FTIII cells areillustrated by solid line histograms.

FIG. 3 illustrates calcium dependence of E-Selectin and P-Selectinbinding to 4T1 cells. FIG. 3A illustrates 4T1 cells stained with humanIgG as a control. FIG. 3B illustrates IgG-chimeric E-Selectin binding inthe absence of EDTA. FIG. 3C illustrates IgG-chimeric E-Selectin bindingin the presence of 10 mM EDTA. FIG. 3D illustrates IgG-chimericP-Selectin binding in the absence of EDTA. FIG. 3E illustratesIgG-chimeric P-Selectin binding in the presence of 10 mM EDTA. FIG. 3Fillustrates IgG-chimeric P-Selectin binding in the presence of 20 mMEDTA. FIG. 3G illustrates IgG-chimeric P-Selectin binding in thepresence of 40 mM EDTA. Mean fluorescence intensity for each histogramis shown.

FIG. 4 illustrates the effect of neuraminadase treatment of 4T1 cells onP-Selectin binding. The heavy line histogram represents staining withsecondary antibody only. The light continuous line histogram representsP-Selectin reactivity without neuraminidase treatment. The dashed linehistogram represents P-Selectin reactivity with neuraminidase treatment.

FIG. 5 illustrates that pronase treatment of 4T1 cells reducesP-Selectin reactivity with the cells. P-Selectin binding to the 4T1cells (thin line histogram) was sharply reduced (dotted line) to thelevel of secondary antibody binding (thick solid line).

FIG. 6 illustrates that inhibition of sulfation decreases P-Selectinbinding to 4T1 cells. FIG. 6A illustrates P-Selectin binding tountreated cells. FIG. 6B illustrates P-Selectin binding to cells treatedto inhibit sulfation.

FIG. 7 illustrates the effect of heparinase and chondroitinase onP-Selectin binding. FIG. 7A illustrates untreated cells. FIG. 7Billustrates P-Selectin binding to untreated cells. FIG. 7C illustratesP-Selectin binding to cells treated with heparinase and chondroitinase.

FIG. 8 illustrates histochemical binding of P-Selectin to the primarymass and metastatic pulmonary tumors. P-Selectin ligands were expresseduniformly and strongly on cells of the primary mass in both parental 4T1cells (FIG. 8A) and sialyl-Lewis X Negative cells (sLe^(x)-Neg) (FIG.8B). P-Selectin ligands were very strongly expressed on metastatic cellsin lung sections (FIG. 8C). Bar equals 20 μm.

FIG. 9 illustrates involvement of P-Selectin ligands in binding to humanvascular endothelial cells. Percentage of adhesion was calculated basedon mean fluorescence intensities and presented as average of 11replications. Bars represent SD based on 11 replications. Arepresentative experiment out of three is shown. Paired Student's t testwas used to compare the means.

FIG. 10 illustrates the effect of heparin on P-Selectin interaction withsLe^(x)-Neg tumor cells. FIG. 10A illustrates the tumor cells incubatedwith secondary antibody alone. FIG. 10B illustrates the interaction ofP-Selectin with the tumor cells when the P-Selectin had beenpre-incubated with 0.7 Units heparin prior to exposure to the cells.FIG. 10C illustrates the interaction of P-Selectin with the tumor cellswhen the P-Selectin had been pre-incubated with 3.0 Units heparin priorto exposure to the cells. FIG. 10D illustrates the interaction ofP-Selectin with the tumor cells when the P-Selectin had beenpre-incubated with 15.0 Units heparin prior to exposure to the cells.FIG. 10E illustrates the interaction of P-Selectin with the tumor cellswhen the P-Selectin had been pre-incubated with 60.0 Units heparin priorto exposure to the cells. FIG. 10F illustrates the interaction ofP-Selectin with the tumor cells when the P-Selectin had beenpre-incubated with 120.0 Units heparin prior to exposure to the cells.

FIG. 11 illustrates that heparin inhibits binding of mouse platelets to4T1 cells. FIG. 11A illustrates lack of binding of 4T1 cells incubatedwith untreated platelets. FIG. 11B illustrates binding of 4T1 cells toplatelets which had been pre-treated with thrombin. FIG. 11C illustratesthat heparin can inhibit binding of 4T1 cells to platelets which hadbeen pre-treated with thrombin.

FIG. 12 illustrates that chondroitin sulfates are P-Selectin ligands on4T1 cells. FIG. 12A illustrates 4T1 cells incubated with secondaryantibody alone. FIG. 12B illustrates P-Selectin binding to 4T1 cells.FIG. 12C illustrates P-Selectin binding to 4T1 cells which had beenpre-treated with heparinase. FIG. 12D illustrates P-Selectin binding to4T1 cells which had been pre-treated with chondroitinase. FIG. 12Eillustrates P-Selectin binding to 4T1 cells which had been pre-treatedwith both heparinase and chondroitinase.

FIG. 13 illustrates inhibition of P-Selectin binding to 4T1 cells bychondroitin sulfate. FIG. 13A illustrates 4T1 cells incubated withsecondary antibody alone. FIG. 13B illustrates P-Selectin binding to 4T1cells. FIG. 13C illustrates P-Selectin binding to 4T1 cells when theP-Selectin had been pre-treated with 5.0 mg/ml chondroitin sulfate A.FIG. 13D illustrates P-Selectin binding to 4T1 cells when the P-Selectinhad been pre-treated with 5.0 mg/ml chondroitin sulfate B. FIG. 13Eillustrates P-Selectin binding to 4T1 cells when the P-Selectin had beenpre-treated with 0.5 mg/ml chondroitin sulfate A. FIG. 13F illustratesP-Selectin binding to 4T1 cells when the P-Selectin had been pre-treatedwith 0.5 mg/ml chondroitin sulfate B. FIG. 13G illustrates P-Selectinbinding to 4T1 cells when the P-Selectin had been pre-treated with 0.05mg/ml chondroitin sulfate A. FIG. 13H illustrates P-Selectin binding to4T1 cells when the P-Selectin had been pre-treated with 0.05 mg/mlchondroitin sulfate B. FIG. 13I illustrates P-Selectin binding to 4T1cells when the P-Selectin had been pre-treated with 0.005 mg/mlchondroitin sulfate A. FIG. 13J illustrates P-Selectin binding to 4T1cells when the P-Selectin had been pre-treated with 0.005 mg/mlchondroitin sulfate B.

FIG. 14 illustrates inhibition of P-Selectin binding to 4T1 cells bychondroitin sulfate. FIG. 14A illustrates 4T1 cells incubated withsecondary antibody alone. FIG. 14B illustrates P-Selectin binding to 4T1cells. FIG. 14C illustrates P-Selectin binding to 4T1 cells when theP-Selectin had been pre-treated with 0.5 mg/ml chondroitin sulfate E.FIG. 14D illustrates P-Selectin binding to 4T1 cells when the P-Selectinhad been pre-treated with 0.05 mg/ml chondroitin sulfate E. FIG. 14Eillustrates P-Selectin binding to 4T1 cells when the P-Selectin had beenpre-treated with 0.005 mg/ml chondroitin sulfate E. FIG. 14F illustratesP-Selectin binding to 4T1 cells when the P-Selectin had been pre-treatedwith 0.0005 mg/ml chondroitin sulfate E.

FIG. 15 illustrates that CS PGs are the main P-Selectin ligands on thesurface of a human breast cancer cell line. Inhibition of P-Selectinbinding to metastatic human breast cancer cells chondroitinase or amixture of glycosaminoglycans and chondroitin sulfate is illustrated.FIG. 15A illustrates MDA-MET cell variant, which is a bone-colonizingvariant of MDA-MB-231 cell line, incubated with secondary antibodyalone. FIG. 15B illustrates P-Selectin binding to MDA-MET cells. FIG.15C illustrates P-Selectin binding to MDA-MET cells when the cells hadbeen pre-treated with heparinase. FIG. 15D illustrates P-Selectinbinding to MDA-MET cells when the cells had been pre-treated withchondroitinase. FIG. 15E illustrates P-Selectin binding to MDA-MET cellswhen the cells had been pre-treated with both heparinase andchondroitinase. FIG. 15F illustrates P-Selectin binding to MDA-MET cellswhen the P-Selectin had been pre-treated with 10.0 mg/ml of achondroitin sulfate and glycosaminoglycan mixture. FIG. 15G illustratesP-Selectin binding to MDA-MET cells when the P-Selectin had beenpre-treated with 1.0 mg/ml of a chondroitin sulfate andglycosaminoglycan mixture.

FIG. 16. Western Blot. A) MDA-MB231 cell lysate subjected to SDS-PAGEand the gel probed with recombinant human P-Selectin (lane 1),anti-NRP-1 (C-19 antibody, lane 2), and anti-chondroitin sulfate-A (2H6antibody, lane 3). B) Immunoprecipitated fraction of cleared MDA-231lysate immunoprecipitated with P-Selectin on protein G beads (DYNA BEADSsystem), probed with anti-NRP-1.

FIG. 17. Western blot. MDA-231 cell lysate was probed with polyclonalanti-Syndecan-4 (lanes 1, 3, and 4) and recombinant human P-Selectin(lane 2). Lanes 1, 2, and 4 are total cell lysate. Lane 3 is theimmunoprecipitated fraction of cleared MDA-231 cell lysateimmunoprecipitated with P-Selectin on protein G beads (DYNA BEADSsystem).

FIG. 18. FACS analysis of M14 melanoma cells, or M14 cells transfectedwith a vector expressing MCSP (M14-MCSP). Cells were analyzed with ananti-CS-A antibody (2H6), anti-MCSP (225.28), or P-Selectin. The controlpanels were M14 cells labeled only with secondary antibody.

FIG. 19. Relative expression of four genes involved in chondroitinsulfate biosynthesis in the cell lines MCF7, MDA-231, MDA-468, andMDA-MET. The ratio of the mRNA as assayed by real-time PCR is shown as aratio to 18S RNA. The raw data were log transformed and subtracted by18S RNA levels for statistical analysis. Comparisons were made by ANOVAand post-hoc analysis and significant differences are shown by letters.

FIG. 20. Chondroitin sulfate inhibits metastasis. Mice were injectedwith 4T1 cells into fact pads. After tumors were palpable (3-4 daysafter transplant) they were daily injected with CS intraperitoneally(ip) or subcutaneously (sc). Micer were sacrificed 30 days aftertransplant and lung colonies were quantified. Saline injection was usedas a control. Comparisons were made between groups treated with CS andthe saline group as control. NS, not significant. Average and SD withthree animals per group is shown.

DETAILED DESCRIPTION Definitions

T cells are considered to specifically recognize a protein or aparticular sequence if the CD4+ or CD8+ T cells show a response whencontacted with antigen-presenting cells or target cells pulsed with apeptide consisting of the sequence. The response may be cytolysis oftarget cells pulsed with the peptide consisting of the sequence, orcytokine release or amplification in response to contactingantigen-presenting cells pulsed with the peptide consisting of thesequence.

Description

In certain embodiments of the present invention, compositions aredisclosed for the inhibition of cancer metastasis. In particularembodiments, such a composition for inhibiting metastasis of a cancercell may comprise a chondroitin sulfate ligand. In other embodiments, acomposition for inhibiting metastasis of a cancer cell may comprise aP-Selectin ligand.

The compositions are pharmaceutical compositions and may comprise apharmaceutically acceptable diluent. The pharmaceutical composition maybe formulated for administration by any suitable route, includingintravenous, subcutaneous, intramuscular, or intraperitoneal injection.The pharmaceutical compositions may also be formulated for oraladministration.

CS proteoglycans on the surface of cancer cells are shown to be majorP-Selectin ligands involved in prometastatic heterotypic adhesion oftumor cells to platelets or endothelial cells. Metastasis may beinhibited by contacting platelets or endothelial cells with a P-Selectinligand thereby preventing the interaction of platelets or endothelialcells with cancer cells. Thus, one aspect of the present inventionprovides for a metastasis inhibiting composition comprising a P-Selectinligand that blocks the binding of P-Selectin to chondroitin sulfate oncancer cells. Such a P-Selectin ligand may be, for example, chondroitinsulfate.

One aspect of the present invention provides for a metastasis inhibitingcomposition comprising chondroitin sulfate. Yet a further aspect of thepresent invention provides for a metastasis inhibiting compositioncomprising a chondroitin sulfate binding agent which blocks the bindingof P-Selectin to chondroitin sulfate. The particular CS that may beuseful according to the present embodiment may be any of a variety of CSmolecules including, but not limited to, CS PGs, CS A, CS B, CS C, CS D,or CS E. Additionally, inhibition of binding of platelets comprisingP-Selectin to cancer cells which comprise cell surface CS PGs can beachieved by contacting the P-Selectin on platelets with free or unboundCS thereby inhibiting metastasis. Similarly, binding of endothelialcells comprising P-Selectin to cancer cells which comprise cell surfaceCS PGs can be blocked by contacting the P-Selectin on endothelial cellswith free or unbound CS thereby inhibiting metastasis. The free orunbound chondroitin sulfate may be free or unbound CS PGs, CS A, CS B,CS C, CS D, or CS E.

In a further aspect of the present invention, binding of P-Selectin toCS PGs on the surface of cancer cells can be prevented by contacting theCS on cancer cells with a chondroitin sulfate ligand or binding agent.Free or unbound P-Selectin or a chondroitin sulfate binding domain ofP-Selectin may be contacted to the cancer cell. In this manner, the freeP-Selectin or chondroitin sulfate binding domain of P-Selectin may bindto the chondroitin sulfate of the cancer cells and prevent theinteraction of cancer cells with cells comprising P-Selectin, such asplatelets or endothelium. Because the chondroitin sulfate of the cancercells is bound, metastasis is inhibited.

The extent of synthesis of chondroitin sulfate and sulfation ofchondroitin sulfate is relevant to the binding of chondroitin sulfate toP-Selectin. Therefore, in certain embodiments of the present invention,a composition for inhibiting metastasis of a cancer cell may comprise aninhibitor of synthesis chondroitin sulfate. Such an inhibitor wouldinclude an inhibitor of sulfation of chondroitin sulfate. By decreasingthe synthesis or sulfation of chondroitin sulfate on tumor cells, thebinding of chondroitin sulfate by P-Selectin is limited. As a result, itis possible to limit the metastasis of a cancer cell by inhibitingsulfation of chondroitin sulfate.

In various embodiments of the present invention, methods of inhibitingmetastasis are disclosed. In one embodiment, a method of inhibitingmetastasis comprises blocking the interaction of a first cell comprisingchondroitin sulfate with a second cell by contacting said first cellwith a chondroitin sulfate ligand.

In another embodiment of the present invention, a method of inhibitingmetastasis may comprise blocking the interaction of a first cellcomprising chondroitin sulfate with a second cell comprising P-Selectinby contacting said second cell with a P-Selectin ligand.

In various aspects of the present invention, methods are disclosed toinhibit metastasis by inhibiting the interaction of P-Selectin expressedon platelets or endothelium with chondroitin sulfate proteoglycansexpressed on tumor cells.

In various aspects of the present invention, methods are disclosed toinhibit metastasis by inhibiting the interaction of P-Selectin expressedon endothelial cells with chondroitin sulfate proteoglycans expressed ontumor cells.

In yet another aspect of the present invention, binding of P-Selectin onplatelets or P-Selectin on endothelial cells to CS PGs on the surface ofcancer cells can be prevented by contacting the CS PGs on the surface ofcancer cells with a chondroitin sulfate binding agent that inhibits orblocks the P-Selectin binding site. Such a chondroitin sulfate ligand orbinding agent would be, such as, for example, free P-Selectin or suchas, for example, anti-CS antibodies.

In a further aspect of the present invention, CS can be utilized tostimulate an immune response, thereby inducing CS-specific antibodiesthat block the interaction of P-Selectin with CS bound to tumor cells.Antibodies for such a strategy may be generated in vivo or in vitro.Such antibodies inhibit metastasis via active immunization or passiveimmunization.

In particular embodiments of the present invention, a method ofinhibiting metastasis may comprise contacting a cancer cell with achondroitin sulfate synthesis or sulfation inhibitor. It is within thescope of the present invention that disruption of the enzymatic pathwaysthat result in CS production or other cellular pathways that result inP-Selectin production may be useful for inhibiting the interaction of CSof tumor cells with P-Selectin of platelets or P-Selectin of endothelialcells thereby inhibiting metastasis. In particular, a method ofinhibiting metastasis may comprise contacting a cancer cell with achondroitin sulfate synthesis or chondroitin sulfate sulfationinhibitor. Such an inhibitor may inhibit sulfation of chondroitinsulfate, thereby inhibiting the effectiveness of P-Selectin binding tochondroitin sulfate. As a result, metastasis is inhibited. Exemplaryinhibitors include inhibitors of cellular enzymes that are involved inthe synthesis of chondroitin sulfate. Particular enzymes include, butare not limited to, chondroitin synthase, chondroitinN-acetylgalactosaminyltransferase (Chondroitin GalNAcT),chondroitin-glucuronate C5-epimerase, chondroitin 4-O-sulfotransferase-1(C4ST1), chondroitin 4-O-sulfotransferase-2 (C4ST2), chondroitin4-O-sulfotransferase-3 (C4ST3), dermatan 4-O-sulfotransferase-1 (D4ST1),chondroitin 6-O-sulfotransferase (C6ST), chondroitin6-O-sulfotransferase-2 (C6ST2), chondroitin 4-sulfate6-O-sulfotransferase (GalNAc4S-6ST) and galactosaminyl uronyl 2-0sulfotransferase (CS/DS2ST). Inhibition of any of these enzymes may beachieved by any of a variety of compositions and methods. For example,small molecule inhibitors of an enzyme may be used. Alternatively, theexpression of particular enzymes may be down-regulated through molecularbiology techniques that are commonly known to one of skill in therelevant art. For example, anti-sense RNAs from anti-sense constructs orsiRNA (short interfering RNAs) may be used to disrupt translation andthereby inhibit expression.

It is within the scope of various aspects of this invention thatmetastasis may be inhibited for numerous cancers including, but notlimited to, cancers selected from the group consisting of colon cancer,lung cancer, breast cancer, malignant melanoma, gastric cancer, tonguesquamous cancer, myeloma and neuroblastoma.

In various aspects of the present invention, methods are disclosed toinhibit metastasis by inhibiting the interaction of P-Selectin expressedon platelets with chondroitin sulfate proteoglycans expressed on tumorcells. In various aspects of the present invention, methods aredisclosed to inhibit metastasis by inhibiting the interaction ofP-Selectin expressed on endothelial cells with chondroitin sulfateproteoglycans expressed on tumor cells.

In one aspect of the present invention, CS proteoglycans on the surfaceof cancer cells are shown to be major P-Selectin ligands involved inprometastatic heterotypic adhesion of tumor cells to platelets orendothelial cells. In another aspect of the present invention,metastasis may be inhibited by contacting platelets or endothelial cellswith a P-Selectin ligand thereby preventing the interaction of plateletsor endothelial cells with cancer cells.

In a further aspect of the present invention, binding of P-Selectin toCS PGs on the surface of cancer cells can be prevented by contacting theP-Selectin with free or unbound CS thereby inhibiting metastasis.Additionally, inhibition of binding of platelets or endothelium whichcomprise P-Selectin to cancer cells which comprise cell surface CS PGscan be achieved by contacting the P-Selectin on platelets with free orunbound CS. The free or unbound chondroitin sulfate may be free orunbound CS PGs, CS A, CS B, CS C, CS D, CS E.

In yet a further aspect of the present invention, binding of P-Selectinto CS PGs on the surface of cancer cells can be prevented by contactingthe P-Selectin with a P-Selectin ligand, such as a small molecule, thatprevents, blocks or inhibits binding of P-Selectin to CS therebyinhibiting metastasis. Additionally, inhibition of binding of plateletswhich comprise P-Selectin to cancer cells which comprise cell surface CSPGs can be achieved by contacting the P-Selectin on platelets with aP-Selectin ligand that prevents, blocks or inhibits binding ofP-Selectin to CS, thereby inhibiting metastasis. Similarly, binding ofendothelial cells which comprise P-Selectin to cancer cells whichcomprise cell surface CS PGs can be achieved by contacting theP-Selectin on endothelial cells with a P-Selectin ligand that prevents,blocks or inhibits binding of P-Selectin to CS thereby inhibitingmetastasis. It is also envisioned within the scope of the presentinvention that modified forms of CS chains with improved specificity forP-Selectin or peptides that mimic the clustering structure of tumor cellsurface CS may also be used for inhibition of metastasis.

It is within the scope of the various compositions and methods of thisinvention that metastasis may be inhibited for numerous cancersincluding, but not limited to, cancers selected from the groupconsisting of colon cancer, lung cancer, breast cancer, malignantmelanoma, gastric cancer, tongue squamous cancer, myeloma andneuroblastoma. It also may be inhibited for other cancers, including butnot limited to prostate cancer.

Another embodiment of the invention provides a method of identifying acandidate drug to treat cancer (or inhibit metastasis) comprising:testing one or more compounds for inhibiting a chondroitin sulfatesynthesis enzyme to identify a compound that inhibits a chondroitinsulfate synthesis enzyme; wherein a compound that inhibits a chondroitinsulfate synthesis enzyme is a candidate drug to treat cancer (or inhibitmetastasis).

In particular embodiments, the CS synthesis enzyme is selected from thegroup consisting of: chondroitin synthase, chondroitinN-acetylgalactosaminyltransferase (Chondroitin GalNAcT),chondroitin-glucuronate C5-epimerase, chondroitin 4-O-sulfotransferase-1(C4ST1), chondroitin 4-O-sulfotransferase-2 (C4ST2), chondroitin4-O-sulfotransferase-3 (C4ST3), dermatan 4-O-sulfotransferase-1 (D4ST1),chondroitin 6-O-sulfotransferase (C6ST), chondroitin6-O-sulfotransferase-2 (C6ST2), chondroitin 4-sulfate6-O-sulfotransferase (GalNAc4S-6ST) and galactosaminyl uronyl 2-Osulfotransferase (CS/DS2ST).

In other particular embodiments, the CS synthesis enzyme is selectedfrom the group consisting of: chondroitin synthase,chondroitin-glucuronate C5-epimerase, chondroitin 4-O-sulfotransferase-1(C4ST1), chondroitin 4-O-sulfotransferase-2 (C4ST2), chondroitin4-O-sulfotransferase-3 (C4ST3), chondroitin 6-O-sulfotransferase (C6ST),chondroitin 6-O-sulfotransferase-2 (C6ST2), chondroitin 4-sulfate6-O-sulfotransferase (GalNAc4S-6ST) and galactosaminyl uronyl 2-Osulfotransferase (CS/DS2ST).

In another embodiment, the chondroitin synthesis enzyme is chondroitinN-acetylgalactosaminyltransferase (Chondroitin GalNAcT), which isreported to transfer beta1,4-N-acetylgalactosamine (GalNAc) fromUDP-[(3)H]GalNAc to a polymer chondroitin (beta-GalNAc transferase IIactivity. (Uyama T, Kitagawa H, Tamura Ji J, Sugahara K. Molecularcloning and expression of human chondroitinN-acetylgalactosaminyltransferase: the key enzyme for chain initiationand elongation of chondroitin/dermatan sulfate on the protein linkageregion tetrasaccharide shared by heparin/heparan sulfate. J Biol Chem.2002 Mar. 15; 277(11):8841-6.)

In another embodiment, the chondroitin synthesis enzyme is dermatan4-O-sulfotransferase-1 (D4ST1), works following the epimerase that makescs-b. D4ST-1 is reported to transfer sulfate to GalNAc residues in-IdoUA-Gal-NAc-IdoUA- and -GlcUA-GalNAc-GlcUA-sequences.

Chondroitin 6-O-sulfotransferase (C6ST) (EC:2.8.2.17) catalyzes additionof a sulfate on carbon 6 of the NAcetylgalactosamine residues ofchondroitin. Galactosaminyl uronyl 2-O-sulfotransferase (CS/DS2ST)oversulfates CS-B. Chondroitin 4-sulfate 6-O-sulfotransferase(GalNAc4S-6ST) (EC:2.8.2.33) adds a sulfate to the 6 position ofchondroitin 4-sulfate.

Key CS synthesis enzymes are listed in Tables 1 and 2.

TABLE 1 Chondroitin sulfate types and key enzymes in the pathwayChondroi- tin type Disaccharide Modifying enzymes product repeatsubstrate Sulfotransferase Epimerase A [GlcUAβ1- Chondroitin-4 —3GalNAc(4S)] sulfotransferase 11, 12, 13 B [IdoUA(2S)α1-Uronyl-2-sulfotransferase and dermatan 3GalNAc(4S)] chondroitin-4sulfotransferase sulfate 11, 12, 13 epimerase C [GlcUAβ1-N-acetylglucosamine-6-O — 3GalNAc(6S)] sulfotransferase 7 D[GlcUA(2S)β1- Uronyl-2-sulfotransferase and — 3GalNAc(6S)]N-acetylglucosamine 6-O sulfotransferase 7 E [GlcUAβ1- Chondroitin-4sulfotransferase — 3GalNAc(4S,6S)] 11, 12, 13 and N- acetylgalactosamine4-sulfate 6-O-sulfotransferase iE [IdoUAα1- Chondroitin-4sulfotransferase dermatan 3GalNAc(4S,6S)] 11, 12, 13 and N- sulfateacetylgalactosamine epimerase 4-sulfate 6-O-sulfotransferase

TABLE 2 Genes involved in biosynthesis of human CS types. RefSeqAccession Gene Name Full Name Enzyme NM_018413 CHST11 Chondroitin 4-O-EC: 2.8.2.5 sulfotransferase 11 (C4ST1) NM_018641 CHST12 Chondroitin4-O- EC: 2.8.2.5 sulfotransferase 12 (C4ST2) NM_152889 CHST13Chondroitin 4-O- EC: 2.8.2.5 sulfotransferase 13 (C4ST3) NM_004273 CHST3Chondroitin 6-O- EC: 2.8.2.17 sulfotransferase 3 NM_014918 CHSY1Chondroitn synthase 1 EC: 2.4.1.175 EC: 2.4.1.226 NM_015892 GALNAC4S-Chondroitin 4-sulafte EC: 2.8.2.33 6ST 6-O-sulfotransferase NM_013352SART2 or Squamous cell carcinoma EC: 5.1.3.19 DS-epimerase antigenrecognized by T cells 2 or Dermatan sulfate-5-epimerase

It is shown below in Example 21 that CHST11, also known as C4ST1, isvery highly expressed in highly aggressive breast cancer cells. This isfurther evidence linking chondroitin sulfate synthesis and in particularC4ST to metastasis. Thus, a compound that inhibits an enzyme in thepathway for synthesis of chondroitin sulfate is expected to inhibitmetastasis.

Methods are known in the art to screen a library of compounds orindividual compounds for inhibition of enzymes. One simple way to screenfor inhibitors of chondroitin synthesis enzyme is to screen wells of amultiwell plate where each well is treated with a different compound,screening with an antibody against CS (see, e.g., Uyama, T. et al., J.Biol. Chem. 281:38668-38674). It is shown below in Example 14 that CS-Band CS-E inhibited P-Selectin binding to tumor cells more than CS-A andCS-C. Thus, it may be advantageous to screen with an antibody againstCS-E or CS-B specifically.

Inhibition of particular enzymes involved in CS synthesis may be assayedin vitro with purified enzyme or crude extracts containing the enzyme ofinterest using appropriate radioactively labeled substrate. Forinstance, chondroitin-glucuronate C5-epimerase activity may be assayedusing 5-³H-labeled glucuronic acid residues and assaying for release of³H₂O. (Li, J-P et al., 2001, J. Biol. Chem. 276:20069-20077; Campbell,P. et al., 1994, J. Biol. Chem. 269:26953-26958; Li, J. P. et al., 1997,J. Biol. Chem. 272:28158-28163.) Chondroitin-glucuronate C5-epimerase isof particular interest because it is involved specifically in synthesisof CS-B.

Chondroitin 4-sulfate 6-O-sulfotransferase, also known asN-acetylgalactosamine 4-sulfate 6-O-sulfotransferase (GalNAc4S-6ST),transfers a sulfate from 3′-phosphoadenosine 5′-phosphosulfate (PAPS) toposition 6 of N-acetylgalactosamine 4-sulfate in chondroitin sulfate. Itcan be assayed in an assay mixture with [³⁵S]PAPS and CS-A assubstrates, assaying for ³⁵S-labeled glycosaminoglycans (Ito, Y. et al.,2000, J. Biol. Chem. 275:34728-34736). GalNAc4S-6ST is of particularinterest because it is involved specifically in synthesis of CS-E.

Antibodies are also available that are specific for different types ofCS, e.g., CS-A, CS-E, and CS-B, which can be used to detect the productsof the enzyme reactions in order to screen for inhibitors.

Another embodiment of the invention provides a method of identifying acandidate drug to inhibit metastasis comprising: (a) testing one or morecompounds for binding to Melanoma Chondroitin Sulfate Proteoglycan,Syndecan-1, Syndecan-4, or Neuropilin-1 to identify a compound thatbinds to Melanoma Chondroitin Sulfate Proteoglycan, Syndecan-1,Syndecan-4, or Neuropilin-1; wherein a compound that binds to MelanomaChondroitin Sulfate Proteoglycan, Syndecan-1, Syndecan-4, orNeuropilin-1 is a candidate drug to treat cancer. The candidate drugshould bind to MCSP, Syndecan-1, Syndecan-4, or Neuropilin-1 in theirforms with CS attached to the protein.

In particular embodiments, the compound that binds one of the proteinsis an antibody against the protein. Suitable antibodies may bepolyclonal or monoclonal. They may be an antibody fragment. They may behumanized antibodies.

Methods of identifying compounds that bind to MCSP, Syndecan-1,Syndecan-4, or Neuropilin-1 are known to persons of skill in the art.One method is to immobilize MCSP, Syndecan-1, Syndecan-4, orNeuropilin-1 on a solid surface, and assay the ability of a testcompound to compete with soluble P-Selectin for binding to theimmobilized protein. This can be done with a labeled P-Selectin asdescribed in the Examples below. Alternatively, a competitive bindingassay can be done assaying competition of the test compound againstbinding of a polyclonal or monoclonal antibody specific for theimmobilized protein.

In particular embodiments, the compound is a peptide of less than 100amino acid residues. In other embodiments, it is a small molecule ofmolecular weight less than 3,000, which may be non-peptidyl.

In other specific embodiments, the compound is an antibody.

One embodiment of the invention provides a method of inhibitingmetastasis in a mammal afflicted with cancer or suspected to beafflicted with cancer comprising: (a) administering to the mammal anantibody against, or T cells that specifically recognize, MelanomaChondroitin Sulfate Proteoglycan (MCSP), Syndecan-1, Syndecan-4, orNeuropilin-1; or (b) vaccinating the mammal with MCSP, Syndecan-1,Syndecan-4, Neuropilin-1, or a peptide thereof.

Antibodies against MCSP, Syndecan-1, Syndecan-4, or Neuropilin-1 can beprepared as described below.

T cells can be amplified ex vivo as described below. Amplified T cellsthat specifically recognize a particular antigen (MCSP, Syndecan-1,Syndecan-4, or neuroplin-1) can be infused into a patient to mount aresponse against that antigen that inhibits metastasis.

Vaccinating a mammal with MCSP, Syndecan-1, Syndecan-4, Neuropilin-1, ora peptide thereof may involve vaccinating the mammal with the wholeprotein, or with a peptide of the protein. The peptide may be part offusion protein with other sequences. The protein or peptide may be mixedwith an adjuvant to enhance the immune response. Various adjuvantsincluding Freund's complete or incomplete adjuvants are known in theart.

The protein or peptide may also be on antigen-presenting cells when itis used to vaccinate the mammal. The most active antigen-presentingcells are dendritic cells, whose preparation is described below.

Reducing expression of MCSP, Syndecan-1, Syndecan-4 or Neuropilin-1 is ameans to reduce chondroitin sulfate on tumor cells. That is, withoutthese proteins, there are fewer proteins to attach chondroitin sulfateto, and therefore fewer CS ligands on the cancer cell available to bindto P-Selectin. Expression of the proteins can be reduced by smallinterfering RNAs (siRNA) targeted to the genes for MCSP (NM_001897.4),Syndecan-1 (NM_001006946.1), Syndecan-4 (NM_002999.2), or Neuropilin-1(NM_003873.5). Likewise, siRNA can target a gene for a CS synthesisenzyme. Vectors and techniques for gene siRNA silencing of genes aredisclosed in (17-20).

Thus, one embodiment of the invention provides a method of treatingcancer or inhibiting metastasis comprising: administering to a mammalafflicted with cancer a nucleic acid vector adapted to express an siRNAtargeting MCSP, Syndecan-1, Syndecan-4, or Neurpolin-1.

Another embodiment of the invention provides a method of treating canceror inhibiting metastasis comprising: administering to a mammal afflictedwith cancer a nucleic acid vector adapted to express an siRNA targetinga gene for a CS synthesis enzyme.

Another embodiment of the invention provides a method of screening foran agent to inhibit cancer metastasis comprising: testing one or morecompounds not previously known to treat cancer for effect on methylationof DNA to identify an agent that causes hypermethylation of DNA; testingthe agent for inhibition of cancer metastasis in vivo in a mammal.

“Methylation” as used herein refers to methylation of the 5-carbon ofcytosine on CpG dinucleotides in DNA by enzymatic means.

It is shown herein that expression of MCSP, Syndecan-1, Neuropilin-1,and C4ST are all under methylation control. That is, methylation reducesexpression of these genes. Thus, although methylation is usually thoughtof as causing cancer or increasing the risk of cancer, in the case ofthese genes, hypermethylation reduces their expression, and thus reducesthe metastatic potential of a cancer.

Thus, agents that increase methylation are expected to reduce expressionof each of these proteins and thus reduce metastasis.

Agents that cause decreased methylation are known. These hypomethylatingagents include aza-deoxycytidine, aza-cytidine, and aza-dCTP (availablefrom Methylation, Ltd., Port Orange, Fla.).

Hypermethylating drugs are less well known. Instead anticancer researchhas focused on drugs that reduce methylation (Yu N, Wang M. Anticancerdrug discovery targeting DNA hypermethylation. Curr Med Chem. 2008;15(14):1350-75).

Methylation can be assayed as described in Patra S K, et al. 2002 (DNAmethyltransferase and demethylase in human prostate cancer, MolCarcinog. 2002, 33(3):163-71). Screening for agents that causehypermethylation (which may be by inhibition of demethylating enzyme oractivation of a methylating enzyme) can be done by testing forinhibition of methylation or demethylation as described in Patra S K, etal. 2002 (DNA methyltransferase and demethylase in human prostatecancer, Mol Carcinog. 2002, 33(3):163-71). In brief, cultured cells(e.g., cancer cell lines) are washed and broken in lysis buffercontaining detergent. Protein is quantified and a constant amount ofcrude lysis extract is placed in each well of a multiwell plate. Forassay of methylation, 20 μg protein is incubated for 2 hours at 37° C.with pol(dI-dC) or poly(dG-dC) substrate (15 μg) in reaction buffer with2 μCi of ³H-labeled S-adenosylmethionine. The reaction is stopped byadding 300 μl of 1% SDS, 2 mM EDTA, 3% 4-aminosalicylate, 5% butanol,125 mM NaCl, 0.25 mg/ml carrier salmon testis DNA, and 1 mg/mlproteinase K. Protein is extracted with 88% phenol, 12% m-cresol, and0.1% 8-hydroxyquinoline. The reacted DNA template is recovered byethanol precipitation from the aqueous phase. DNA is filtered on Whatman(GF/C) filters and washed with 5% trichloroacetic acid followed by 70%ethanol. Filters are counted by scintillation counting.

For the demethylation assay, 20-25 μg of poly(dI-dC) or poly(dG-dC) islabeled by incubation with 100 μg of cancer cell extract with 10 μCi³H-labeled S-adenosylmethionine overnight at 37° C. The reaction isterminated and nucleic acids are precipitated and dissolved in reactionbuffer. Unincorporated radioactive substances are removed bychromatography through a NAP-5 (Amersham) column. Purified radioactiveDNA is quantified radioactively, and 20,000 cpm is incubated with cellor tissue extracts and released radioactive CH₃OH is counted as ameasure of demethylase activity.

DNA methylation levels at CpG sites of specific genes can be quantified,using bisulfite genomic sequencing followed by methods of quantitativeanalysis for these sequences. (Leakey T I et al. A simple algorithm forquantifying DNA methylation levels on multiple independent CpG sites inbisulfite genomic sequencing electropherograms. Nucleic Acids Res. 2008June; 36(11):e64. Thomas sin H, Kress C, Grange T. MethylQuant: asensitive method for quantifying methylation of specific cytosineswithin the genome. Nucleic Acids Res. 2004 Dec. 2; 32(21):e168.)

P-Selectin binding to CS ligands on cancer cells also reducesangiogenesis and tumor growth, in addition to reducing metastasis. Thus,the methods described herein, in addition to being methods forinhibiting metastasis, are methods to treat cancer, reduce tumor growth,or reduce tumor angiogenesis.

T Cell and Dendritic Cell Culture, Amplification, and Assay.

Dendritic cells can be cultured, and T cells can be cultured, activated,and assayed, as described in International Application PCT/US07/024300.

Dendritic Cell and T Cell Culture.

Peripheral blood mononuclear cells are recovered from peripheral bloodby gradient centrifugation (Lymphoprep; Greiner Bio-One, Longwood,Fla.).

For preparation of dendritic cells, peripheral blood mononuclear cellsare placed in six-well plates (Costar, Cambridge, Mass.) at aconcentration of 5×10⁶ per well in AIM-V medium. After incubation for 2to 3 hours at 37° C., nonadherent cells were removed from the cultureand the medium was replaced with AIM-V plus 800 units/mL granulocytemacrophage colony-stimulating factor and 500 units/mL IL-4. On days 3and 5, half the medium is removed and replaced with AIM-V plus 800units/mL granulocyte macrophage colony-stimulating factor and 500units/mL IL-4. A mix of maturation cytokines (1 μmol/L/mL prostaglandinE2, 1,000 units/mL tumor necrosis factor-∀, and 500 units/mL IL-1β) isadded on day 5 or 6. For stimulation of T cells specific for a peptide,mature dendritic cells are collected after maturation for 48 hours, andpulsed with 50 μg/mL of peptide for 2 hours in AIM-V at 37° C. Thedendritic cells are then washed once with AIM-V medium and used for Tcell stimulation at a peripheral blood mononuclear cell/dendritic cellratio of 30:1. After 7 days, T cells were collected and restimulatedwith peptide-pulsed dendritic cells. After the second stimulation, CD8+or CD4+ T cells may optionally be specifically purified and recovered bypositive selection with anti-CD8 or anti-CD4 magnetic beads (DynalBiotech, Brown Deer, Wis.). During the second and third T cellstimulation and passage, 50 to 100 units/mL IL-2 is added to the medium,and T cells are periodically fed (every 2-3 days) by changing 50% to 70%of the medium and addition of fresh IL-2. Further passaging of CD8+ Tcell lines uses peptide-loaded autologous peripheral blood lymphocytesas antigen-presenting cells.

Cytotoxicity Assays.

Standard ⁵¹Cr-release assays are done as described previously (16).Autologous lymphoblastoid cell lines are pulsed with 50 μg/mL ofappropriate target peptide, or left unpulsed. Lymphoblastoid cell linesare pulsed overnight with 50 μg/mL of peptide at 37° C. in AIM-V medium,whereas dendritic cells are pulsed with 50 μg/mL peptide for 48 hoursduring final maturation. Peptide-pulsed targets were then labeled with50 μCi Na₂[⁵¹Cr]O₄ for an additional hour and washed three times beforeuse. Target cells were plated at 1×10⁴ per well in 96-wellround-bottomed plates with effector T cells.

Raising Antibodies

To generate antibodies, MCSP, Syndecan-1, Syndecan-4, or Neuropilin canbe administered directly to a mammal, or the proteins or peptidefragments thereof can be coupled to a carrier protein. Suitable carrierproteins include keyhole limpet hemocyanin, bovine serum albumin, andovalbumin. Methods of coupling to the carrier protein include singlestep glutaraldehyde coupling and other methods disclosed in Harlow, Edet al., Antibodies: a laboratory manual, Cold Spring Harbor Laboratory(1988).

The immunogen is used to immunize a vertebrate animal in order to inducethe vertebrate to generate antibodies. Preferably the immunogen isinjected along with an adjuvant such as Freund's adjuvant, to enhancethe immune response. Suitable vertebrates include rabbits, mice, rats,hamsters, goats, and chickens.

Hybridomas to synthesize monoclonal antibodies can be prepared bymethods known in the art. See, for instance, Wang, H., et al., AntibodyExpression and Engineering, Am. Chem. Soc., Washington, D.C. (1995).Polyclonal and monoclonal antibodies can be isolated by methods known inthe art. See, for instance, id. and Harlow et al.

Native antibodies are tetramers of two identical light (L) chains andtwo identical heavy (H) chains. The L and H chains each have variabledomains that are responsible for antigen recognition and binding. Thevariability in the variable domains is concentrated in thecomplementarity determining regions (CDRs).

An antibody that is contemplated for use in the present invention can bein any of a variety of forms, including a whole immunoglobulin, anantibody fragment such as Fv, Fab, and similar fragments, a single chainantibody that includes the CDR, and like forms, all of which fall underthe broad term “antibody” as used herein.

The term “antibody fragment” refers to an antigen-binding portion of afull-length antibody. Antibody fragments can be as small as about 4amino acids, about 10 amino acids, or about 30 amino acids or more. Sometypes of antibody fragments are the following:

(1) Fab is the fragment that contains a monovalent antigen-bindingfragment of an antibody molecule. A Fab fragment can be produced bydigestion of whole antibody with the enzyme papain to yield an intactlight chain and a portion of one heavy chain. Two Fab fragments areobtained per whole antibody molecule.

(2) Fab′ is the fragment of an antibody that can be obtained by treatingwhole antibody with pepsin, followed by reduction to yield an intactlight chain and a portion of the heavy chain. Two Fab′ fragments areobtained per whole antibody molecule. Fab′ fragments differ from Fabfragments by the addition of a few residues at the carboxyl terminus ofthe heavy chain CH1 domain including one or more cysteines.

(3) F(ab′)₂ is the fragment that can be obtained by digestion of wholeantibody with pepsin, without reduction. F(ab′)₂ is a dimer of two Fab′fragments held together by two disulfide bonds.

(4) Fv is the minimum antibody fragment that contains a complete antigenrecognition and binding site. Fv consists of a dimer of one H and one Lchain variable domain in a tight, non-covalent association (V_(H)-V_(L)dimer). It is in this configuration that the three CDRs of each variabledomain interact to define an antigen-binding site. Collectively, the sixCDRs confer antigen binding specificity to the antibody. However, even asingle variable domain (or half of an Fv comprising only three CDRsspecific for an antigen) has the ability to bind antigen, although at alower affinity than the complete binding site.

(5) A single chain antibody (SCA) is defined as a genetically engineeredmolecule containing the variable region of the light chain and thevariable region of the heavy chain linked by a suitable polypeptidelinker as a genetically fused single chain molecule.

The preparation of polyclonal antibodies is well known to those skilledin the art. See, for example, Coligan et al., in Current Protocols inImmunology, section 2.4.1 (1992). The preparation of monoclonalantibodies is likewise conventional. See, for example, Harlow et al.,page 726.

Methods of in vitro and in vivo manipulation of monoclonal antibodiesare well known to those skilled in the art. For example, the monoclonalantibodies to be used in accordance with the present invention may bemade by the hybridoma method first described by Kohler and Milstein,Nature 256:495 (1975), or may be made by recombinant methods, e.g., asdescribed in U.S. Pat. No. 4,816,567. The monoclonal antibodies for usewith the present invention may also be isolated from phage antibodylibraries using the techniques described in Clarkson et al., Nature352:624 (1991), as well as in Marks et al., J. Mol. Biol. 222:581(1991). Another method involves humanizing a monoclonal antibody byrecombinant means to generate antibodies containing human specific andrecognizable sequences. See, for review, Holmes et al., J. Immunol.158:2192 (1997) and Vaswani et al., Annals Allergy, Asthma & Immunol.81:105 (1998).

The monoclonal antibodies herein specifically include “chimeric”antibodies in which a portion of the heavy and/or light chain isidentical with or homologous to corresponding sequences in antibodiesderived from a particular species or belonging to a particular antibodyclass or subclass, while the remainder of the chain(s) are identicalwith or homologous to corresponding sequences in antibodies derived fromanother species or belonging to another antibody class or subclass, aswell as fragments of such antibodies, so long as they exhibit thedesired biological activity (U.S. Pat. No. 4,816,567; Morrison et al.,Proc. Nat'l. Acad. Sci. 81:6851 (1984)).

Methods of making antibody fragments are also known in the art (see, forexample, Harlow and Lane, Antibodies: a Laboratory Manual, Cold SpringHarbor Laboratory, New York (1988)). Antibody fragments of the presentinvention can be prepared by proteolytic hydrolysis of the antibody orby expression in E. coli of DNA encoding the fragment. Antibodyfragments can be obtained by pepsin or papain digestion of wholeantibodies by conventional methods. For example, antibody fragments canbe produced by enzymatic cleavage of antibodies with pepsin to provide a5S fragment denoted F(ab′)₂. This fragment can be further cleaved usinga thiol reducing agent, and optionally a blocking group for thesulfhydryl groups resulting from cleavage of disulfide linkages, toproduce 3.5 S Fab′ monovalent fragments. Alternatively, an enzymaticcleavage using pepsin produces two monovalent Fab fragments and an Fcfragment directly. These methods are described, for example, in U.S.Pat. Nos. 4,036,945, and 4,331,647, and references contained therein.

Other methods of cleaving antibodies, such as separation of heavy chainsto form monovalent light-heavy chain fragments, further cleavage offragments, or other enzymatic, chemical, or genetic techniques may alsobe used, so long as the fragments bind to the antigen that is recognizedby the intact antibody. For example, Fv fragments comprise anassociation of V_(H) and V_(L) chains. This association may benoncovalent or the variable chains can be linked by an intermoleculardisulfide bond or cross-linked by chemicals such as glutaraldehyde.Preferably, the Fv fragments comprise V_(H) and V_(L) chains connectedby a peptide linker. These single-chain antigen binding proteins (sFv)are prepared by constructing a structural gene comprising DNA sequencesencoding the V_(H) and V_(L) domains connected by an oligonucleotide.The structural gene is inserted into an expression vector, which issubsequently introduced into a host cell such as E. coli. Therecombinant host cells synthesize a single polypeptide chain with alinker bridging the two V domains. Methods for producing sFvs aredescribed, for example, by Whitlow et al., Methods: a Companion toMethods in Enzymology, 2:97 (1991); Bird et al., Science 242:423 (1988);Ladner et al., U.S. Pat. No. 4,946,778; and Pack et al., Bio/Technology11:1271 (1993).

Another form of an antibody fragment is a peptide containing a singlecomplementarity-determining region (CDR). CDR peptides (“minimalrecognition units”) are often involved in antigen recognition andbinding. CDR peptides can be obtained by cloning or constructing genesencoding the CDR of an antibody of interest. Such genes are prepared,for example, by using the polymerase chain reaction to synthesize thevariable region from RNA of antibody-producing cells. See, for example,Larrick et al., Methods: a Companion to Methods in Enzymology, 2:106(1991).

The invention contemplates human and humanized forms of non-human (e.g.,murine) antibodies. Such humanized antibodies are chimericimmunoglobulins, immunoglobulin chains, or fragments thereof (such asFv, Fab, Fab′, F(ab′)₂ or other antigen-binding subsequences ofantibodies) that contain minimal sequence derived from non-humanimmunoglobulin. For the most part, humanized antibodies are humanimmunoglobulins (recipient antibody) in which residues from a CDR of therecipient are replaced by residues from a CDR of a non-human species(donor antibody) such as mouse, rat, or rabbit having the desiredspecificity, affinity, and capacity.

In some instances, Fv framework residues of the human immunoglobulin arereplaced by corresponding non-human residues. Furthermore, humanizedantibodies may comprise residues that are found neither in the recipientantibody nor in the imported CDR or framework sequences. Thesemodifications are made to further refine and optimize antibodyperformance. In general, humanized antibodies will comprisesubstantially all of at least one, and typically two, variable domains,in which all or substantially all of the CDR regions correspond to thoseof a non-human immunoglobulin and all or substantially all of the FRregions are those of a human immunoglobulin consensus sequence. Thehumanized antibody optimally also will comprise at least a portion of animmunoglobulin constant region (Fc), typically that of a humanimmunoglobulin. For further details, see: Jones et al., Nature 321:522(1986); Reichmann et al., Nature 332:323 (1988); Presta, Curr. OpinionStruct. Biol. 2:593 (1992); Holmes et al., J. Immunol. 158:2192 (1997);and Vaswani et al., Annals Allergy, Asthma & Immunol. 81:105 (1998).

Antibodies of the invention can also be mutated to optimize theiraffinity, selectivity, binding strength or other desirable property. Onemethod of mutating antibodies involves affinity maturation using phagedisplay. Affinity maturation using phage display refers to a processdescribed in Lowman et al., Biochemistry 30:10832 (1991); see alsoHawkins et al., J. Mol. Biol. 254:889 (1992).

Pharmaceutical Compositions

The agents presented herein can be formulated as pharmaceuticalcompositions and administered to a mammalian host, such as a humanpatient in a variety of forms adapted to the chosen route ofadministration, i.e., orally or parenterally, by intravenous,intramuscular, topical or subcutaneous routes.

Thus, the present agents may be systemically administered, e.g., orally,in combination with a pharmaceutically acceptable vehicle such as aninert diluent or an assimilable edible carrier. They may be enclosed inhard or soft shell gelatin capsules, may be compressed into tablets, ormay be incorporated directly with the food of the patient's diet. Fororal therapeutic administration, the agents may be combined with one ormore excipients and used in the form of ingestible tablets, buccaltablets, troches, capsules, elixirs, suspensions, syrups, wafers, andthe like. Such compositions and preparations should contain at least0.1% of agent. The percentage of the compositions and preparations may,of course, be varied and may conveniently be between about 2 to about60% of the weight of a given unit dosage form. The amount of the agentin such therapeutically useful compositions is such that an effectivedosage level will be obtained.

The tablets, troches, pills, capsules, and the like may also contain thefollowing: binders such as gum tragacanth, acacia, corn starch orgelatin; excipients such as dicalcium phosphate; a disintegrating agentsuch as corn starch, potato starch, alginic acid and the like; alubricant such as magnesium stearate; and a sweetening agent such assucrose, fructose, lactose or aspartame or a flavoring agent such aspeppermint, oil of wintergreen, or cherry flavoring may be added. Whenthe unit dosage form is a capsule, it may contain, in addition tomaterials of the above type, a liquid carrier, such as a vegetable oilor a polyethylene glycol. Various other materials may be present ascoatings or to otherwise modify the physical form of the solid unitdosage form. For instance, tablets, pills, or capsules may be coatedwith gelatin, wax, shellac or sugar and the like. A syrup or elixir maycontain the agent, sucrose or fructose as a sweetening agent, methyl andpropylparabens as preservatives, a dye and flavoring such as cherry ororange flavor. Of course, any material used in preparing any unit dosageform should be pharmaceutically acceptable and substantially non-toxicin the amounts employed. In addition, the agent may be incorporated intosustained-release preparations and devices.

The agents may also be administered intravenously or intraperitoneallyby infusion or injection. Solutions of the agents can be prepared inwater, optionally mixed with a nontoxic surfactant. Dispersions can alsobe prepared in glycerol, liquid polyethylene glycols, triacetin, andmixtures thereof and in oils. Under ordinary conditions of storage anduse, these preparations contain a preservative to prevent the growth ofmicroorganisms.

The pharmaceutical dosage forms suitable for injection or infusion caninclude sterile aqueous solutions or dispersions or sterile powderscomprising the active ingredient which are adapted for theextemporaneous preparation of sterile injectable or infusible solutionsor dispersions, optionally encapsulated in liposomes. In all cases, theultimate dosage form should be sterile, fluid and stable under theconditions of manufacture and storage. The liquid carrier or vehicle canbe a solvent or liquid dispersion medium comprising, for example, water,ethanol, a polyol (for example, glycerol, propylene glycol, liquidpolyethylene glycols, and the like), vegetable oils, nontoxic glycerylesters, and suitable mixtures thereof. The proper fluidity can bemaintained, for example, by the formation of liposomes, by themaintenance of the required particle size in the case of dispersions orby the use of surfactants. The prevention of the action ofmicroorganisms can be brought about by various antibacterial andantifungal agents, for example, parabens, chlorobutanol, phenol, sorbicacid, thimerosal, and the like. In many cases, it will be preferable toinclude isotonic agents, for example, sugars, buffers or sodiumchloride. Prolonged absorption of the injectable compositions can bebrought about by the use in the compositions of agents delayingabsorption, for example, aluminum monostearate and gelatin.

Sterile injectable solutions are prepared by incorporating the activeagent in the required amount in the appropriate solvent with various ofthe other ingredients enumerated above, as required, followed by filtersterilization. In the case of sterile powders for the preparation ofsterile injectable solutions, the preferred methods of preparation arevacuum drying and the freeze drying techniques, which yield a powder ofthe active ingredient plus any additional desired ingredient present inthe previously sterile-filtered solutions.

Useful dosages of the anti-cancer agents of the invention can bedetermined by comparing their in vitro activity, and in vivo activity inanimal models. Methods for the extrapolation of effective dosages inmice, and other animals, to humans are known to the art; for example,see U.S. Pat. No. 4,938,949.

The amount of the compound, or an active salt or derivative thereof,required for use in treatment will vary not only with the particularsalt selected but also with the route of administration, the nature ofthe condition being treated and the age and condition of the patient andwill be ultimately at the discretion of the attendant physician orclinician.

EXAMPLES

The following examples are further illustrative of the presentinvention, but it is understood that the invention is not limitedthereto.

The monoclonal antibody KM-93 was purchased from Kamiya Biomedical,Seattle, Wash. The antibodies FH6 and CSLEX1 were purchased fromGlycoTech, Gaithersburg, Md. FITC-conjugated and biotinylated goatanti-mouse IgG or goat anti-mouse IgM were purchased from Sigma.

The murine breast tumor cell line 4T1 was obtained from ATCC (Manassas,Va.). The 4T1 cell line, FTIII transfected 4T1 cell line and pIRES-EGFPtransfected cell line were maintained in DMEM supplemented with 10%fetal bovine serum at 37° C. in sterile culture flasks.

The 1083 bp coding fragment of the human fucosyl transferase III (FTIII)gene (see GenBank Accession Nos. NP_000140 and U27328.1) in pCDNA3plasmid was kindly provided by Dr. Insug O'Sullivan (University ofIllinois). The coding sequence was further adapted for cloning betweenEcoRI and XhoI restriction sites by PCR using the following primers:5′-cgagaattctcaggtgaaccaagccgctatg-3′ (SEQ ID NO.: 1) and5′-cgactcgagatggatcccctgggtgca-3′ (SEQ ID NO.: 2). The amplifiedfragment was digested with EcoRI and XhoI, purified and inserted intothe Multiple Cloning Site (MCS) of pIRES-EGFP vector to makeFTIII-pIRES-EGFP construct. (The pIRES-EGFP vector was obtained from BDBiosciences Clontech (Palo Alto, Calif.).) The 4T1 cells were thentransfected with this construct or pIRES-EGFP vector alone usingLipofectamine™ 2000 (Invitrogen, Carlsbad, Calif.) transfection reagent.The pIRES-EGFP vector contains an internal ribosome entry site (IRES)between the MCS and the EGFP (enhanced green fluorescent protein) codingregion. This allows the FTIII gene (cloned into the MCS) and the EGFPgene to be translated from a single bicistronic mRNA.

Unless specified otherwise, flow cytometry was conducted as follows.Acquisition and analysis of data was performed on an EPICS®™ XL™.flowcytometer (Beckman Coulter, Inc., Fullerton, Calif.). Cells were passedto new flasks 24 hours before measuring lectin binding. The subconfluentmonolayer of cells was detached with Cellstripper (Mediatech, Inc.Herndon, Va.) and washed with Dulbecco's phosphate buffered saline withCa++ and Mg++ (Mediatech, Inc. Herndon, Va.). Cells were transferred toFACS buffer (Dulbecco's Phosphate Buffered Saline, 1% BSA and 0.1%Sodium Azide), counted and diluted to ˜1-2×10⁶/ml. Monoclonal antibodieswere added to a final concentration of 10 μg/ml. Cells were incubated onice for 30 minutes, washed twice with FACS buffer, before the additionof FITC-conjugated streptavidin (2 μg/ml) for lectin analysis orFITC-conjugated goat anti-mouse immunoglobulin for monoclonal analysis.Cells were then washed and fixed with paraformaldehyde, before analysisby flow cytometry.

Recombinant E- and P-Selectin/Fc (human IgG) were purchased from R&Dsystems, Minneapolis, Minn. These recombinant molecules andFITC-conjugated anti-human IgG were used for binding analyses in flowcytometry assays. Human and murine recombinant selectins were used forhuman and murine cells, respectively.

All experiments were repeated at least three times. The Student's t-testor Fisher exact test was used to compare differences between means.Differences were considered significant if P was <0.05.

Example 1

4T1 cells are deficient in sLe^(a) expression making the cell line agood candidate to study the involvement of sLe^(x)-mediated adhesionproperties. There are several monoclonal antibodies (mAbs) defined asKM93, FH6 and CSLEX1 that recognize sLe^(x). These mAbs recognizedifferent forms of the sLe^(x) antigen (1-3). FH6 is specific for anextended form of sLe^(x) (4), while CSLEX1 and KM93 antibodies bothrecognize the sLe^(x) tetrasaccharide. However, the nature of themolecules carrying the carbohydrate determinant is known to affect thereactivity of CSLEX1 and KM93 (5). Among the above antibodies, only KM93reacts with the 4T1 tumor cell surface. KM93, CSLEX-1 or FH6 reactivesLe^(x) epitopes may differentially react with P- and E-Selectin due tovariations in lipid or peptide backbones.

The 4T1 cells were transfected with fucosyltransferase III (FTIII) toexpand the expression of other sLe^(x) epitopes (4T1-FTIII). The 4T1cells were also transfected with pIRES-EGFP vector alone as a control(4T1-EGFP). FIGS. 1A and 1B illustrate 4T1-EGFP cells and 4T1-FTIIIcells, respectively, incubated with secondary antibody alone as control.The binding of KM93 monoclonal antibody was increased on 4T1-FTIII cells(FIG. 1F) relative to 4T1-EGFP (FIG. 1E). More importantly, FH6 reactiveepitopes were expressed at detectable levels in the 4T1-FTIII cells(FIG. 1D) compared to 4T1-EGFP cells (FIG. 1C). Also, CSLEX-1 reactiveepitopes were expressed at detectable levels in the 4T1-FTIII cells(FIG. 1H) compared to 4T1-EGFP cells (FIG. 1G). The antibody bindingdata indicate that transfection with FTIII encoding sequence increasedthe expression of various sLe^(x) epitopes.

Example 2

P-Selectin and E-Selectin reactivity with parental and transfected 4T1cells were examined. Cells were incubated with recombinant mouseE-Selectin/Fc (human IgG) or P-Selectin/Fc (human IgG) chimeras andassayed for binding by flow cytometry. An increase for E-Selectinbinding was observed after FT-III transfection (FIG. 2, first panel).This was expected given the increase in KM93, CSLEX-1 and FH6 bindingafter transfection. P-Selectin, however, bound very well to the parental4T1 cells and the binding did not increase for the transfected cells(FIG. 2, second panel). These data confirm that P-Selectin binding to4T1 cells is not dependent on the expression sLe^(x) on the tumor cellsurface.

Example 3

The dependence of E-Selectin and P-Selectin binding to 4T1 cells ondivalent cation concentration was examined. FIG. 3A illustratesunstained 4T1 cells. FIG. 3B illustrates 4T1 cells incubated withE-Selectin/Fc chimera followed by incubation with FITC-conjugatedanti-human IgG. FIG. 3C is the same as FIG. 3B except the experiment wasconducted in the presence of 10 mM EDTA. Both lectins bind the 4T1cells, with P-Selectin showing very strong reactivity (FIG. 3D).Contrary to the E-Selectin reactivity (see FIGS. 3B and 3C), P-Selectinreactivity was not blocked by a low concentration of EDTA (see FIGS. 3Dand 3E). EDTA inhibited P-Selectin reactivity only at highconcentrations indicating the Ca⁺⁺-independent nature of the reactivity(see FIGS. 3F and 3G).

Example 4

Cells treated with neuraminidase show the relationship betweensialylation and reactivity of P-Selectin. Neuraminidase (Vibriocholerae) was purchased from Sigma (St. Louis, Mo.) and used at aconcentration of 50 mU/ml. Neuraminidase treatment did not change theP-Selectin reactivity (FIG. 4). These results provide further evidencethat E-Selectin and P-Selectin react with separate ligands on thesurface of 4T1 cells. In contrast to E-Selectin, P-Selectin binds tounsialylated ligands on these cells in a Ca²⁺-independent manner.Therefore, sialylated ligands are not a major ligand of P-Selectin inbinding to the 4T1 cells.

Example 5

Cells (4T1) were treated with pronase to determine the proteinaceousnature of P-Selectin ligands. Treatment with pronase dropped theP-Selectin reactivity (dotted histogram) almost to the levels of thenegative control (thick, solid line histogram), indicating theproteinaceous nature of the ligands (FIG. 5). The thin, solid linehistogram represents P-Selectin binding to untreated cells.

Example 6

Sulfated glycosaminoglycans like heparan sulfate and chondroitin sulfateare carbohydrate moieties of proteoglycans, which serve as P-Selectinligands (6, 7). The 4T1 cells were grown in sulfate-free medium in thepresence of sodium chlorate to inhibit sulfate biosynthesis. Cells werewashed with sulfate-free DMEM medium (Hyclone, Logan, Utah) supplementedwith 10% dialyzed FBS and 100 mM sodium chlorate (Sigma) and cultured inthe same medium for 2 hours. The medium was then refreshed andincubation was continued overnight. These treated cells were harvestedwith cell dissociation buffer (Gibco-Invitrogen. Carlsbad, Calif.),washed and resuspended in FACS buffer for further analyses by flowcytometry. Growing the cells in sulfate free medium containing sodiumchlorate led to elimination of P-Selectin binding in a majority of thecells, indicating that most P-Selectin ligands on the 4T1 cells aresulfated (FIG. 6).

Example 7

Treatment of 4T1 cells with a mixture of the glycosaminoglycan-cleavingenzymes, heparinase and chondroitinase, decreased P-Selectin binding(FIG. 7). Removal of glycosaminoglycans was performed by treatment of2×10⁵ cells with a mixture of heparinase II (25 units/ml, Sigma, St.Louis, Mo.) and chondroitinase ABC (5 units/ml, Sigma) in 500 μl of HBSSbuffer for 1 hour at 37° C. Alternatively, the above preparation wastreated with 500 μg pronase (EMD Biosciences, San Diego, Calif.) for 45minutes at 37° C. Removal of sialic acid was performed by incubatingcells with 50 mU/ml neuraminidase from Vibrio cholerae (Sigma) at 37° C.for 1 hour. These data indicate that P-Selectin ligands on the surfaceof 4T1 cells are sulfated proteoglycans, most likely theglycosaminoglycans heparan sulfate or chondroitin sulfate.

Example 8

P-Selectin ligands are stably expressed on the surface of 4T1 cells. Toexamine the stability of expression in vivo, pathological samples fromprimary 4T1 and 4T1 sLe^(x)-Neg variant tumors were stained (FIG. 8).P-Selectin histochemistry was performed as follows: primary tumors andlungs were harvested from mice inoculated with the 4T1 cells at 21 dayspost inoculation, placed in optimal cutting temperature compound (TedPella Inc., Redding, Calif.) and frozen in liquid nitrogen. Five micronfrozen sections were fixed for 10 minutes in cold acetone and thenwashed with cold DPBS (Cellgro® Mediatech, Herndon, Va.). Endogenousperoxidase was blocked by immersion in 0.3% (w/v) hydrogen peroxide inabsolute methanol for 15 minutes followed by DPBS wash. Non-specificbinding was blocked by incubating with DPBS+1% BSA at room temperaturefor 20 minutes. Sections were then incubated with recombinant mouseP-Selectin/human FC chimera (R&D systems, Minneapolis, Minn.) for 30minutes in DPBS+0.2% BSA at room temperature and then washed in DPBS.Sections were incubated with anti-human IgG (Fc specific) peroxidaseconjugate (1/300 dilution) for 15 minutes at room temperature followedby DPBS wash. Sections were incubated with diaminobenzidine solution(DAB) for 5 minutes at room temperature, washed with distilled water,counterstained with methyl green, mounted, and examined under a lightmicroscope. Primary antibody was omitted in negative controls to ruleout non-specific binding of the secondary antibody. P-Selectin ligandswere observed to be significantly and stably expressed on the surface oftumor cells in the primary and secondary lesions, and expression wassimilar for both 4T1 and sLe^(x/a)-Neg variant tumors. Therefore,P-Selectin ligands play a role in hematogenous metastasis in thissyngeneic breast cancer model.

Example 9

Interaction of P-Selectin and its ligands play an important role in 4T1cells binding to HUVECs (FIG. 9). To measure tumor cell adhesion toendothelial cells, Clonetics™ human umbilical vein endothelial cell(HUVEC) system was used (Cambrex Biosciences, Walkersville, Md.). Amonolayer of HUVEC cells was prepared. HUVECs were incubated withsupplied medium supplemented with IL-4 (20 ng/ml) for 24 hours. Mediumwas replaced with similar medium supplemented with Prostaglandin E2(PGE2) for 10 minutes. Calcein AM-labeled (Molecular Probes, Eugene,Oreg.) 4T1 cells were treated with chondroitinase/heparinase, then addedto the activated monolayers of HUVECs. Cells were co-incubated at 37° C.for 30 minutes and then unbound 4T1 cells were removed by washing gentlywith pre-warmed medium. PBS was added to all wells and fluorescencemeasured and percentage of adhesion was calculated. Stimulating surfaceexpression of P-Selectin on HUVECs led to an increase in adhesion to the4T1 cells. The adhesion to 4T1 cells was significantly inhibited bytreatment with the mixture of heparinase and chondroitinase. There wasbackground adhesion to HUVECs, which was also significantly inhibited bytreating the 4T1 cells with heparinase/chondroitinase mix, implying aconstitutive presence of P-Selectin on the HUVECs under our experimentalconditions. This was confirmed by examining P-Selectin expression onHUVECs. A low constitutive expression of P-Selectin was detected on 10%of cells, which was elevated to a more intense staining on about 20% ofcells after treatment with IL-4 and PGE2. Adhesion was clearly enhancedafter P-Selectin induction on HUVECs and suppressed afterheparinase/chondroitinase treatment of tumor cells (FIG. 9).

Example 10

Heparin inhibits both P-Selectin binding to the tumor cells and tumorcell-platelet interactions mediated by P-Selectin. Heparin's ability toinhibit P-Selectin interaction with the cell surface in vitro was testedusing the sLe^(x)-Neg 4T1 cell variant. Recombinant P-Selectin wasincubated with heparin and then the mixture was added to cells to testthe binding (FIG. 10). Heparin efficiently inhibited P-Selectin bindingto cells in a dose dependent manner.

Example 11

To examine if heparin can block the interaction of mouse platelets withtumor cells, 4T1 cells were mixed with Calcein-AM-labeled mouseplatelets in the presence of mouse thrombin with or without heparin.Mouse thrombin was added to stimulate relocation of P-Selectin toplatelet surface and tumor cells were then analyzed by flow cytometryfor Calcein-AM staining, indicating platelet attachment. Thrombintreated platelets showed binding to tumor cells, which was reduced inthe presence of heparin (FIG. 11). Blood was collected into sodiumcitrate (0.38% w/v) from naive mice and platelets were isolated fromplasma by centrifugation. Platelet were washed and labeled with 5 μMfinal Calcein-AM (Molecular Probes, Eugene, Oreg., USA) for 15 minutesat 37° C. Platelets were then washed and incubated with 1 U/ml thrombin(Haematologic Technologies Inc, Essex Junction, Vt.) at 37° C. for 10minutes. Heparin (Baxter Healthcare Corp., Deerfield, Ill., 100 U/mlfinal concentration) was then added to the mixture of platelets andthrombin, and incubated with 4T1 cells in flow cytometry tubes, for 15minutes at room temperature, then acquired and analyzed by flowcytometry.

FIG. 11A illustrates lack of binding of 4T1 cells incubated withuntreated platelets. FIG. 11B illustrates binding of 4T1 cells toplatelets which had been pre-treated with thrombin. FIG. 11C illustratesthat heparin can inhibit binding of 4T1 cells to platelets which hadbeen pre-treated with thrombin. The data illustrate that tumorcell-platelet interaction is P-Selectin mediated and can be blocked byheparin.

Example 12

It has been shown that heparin administration at clinically relevantdose inhibited lung metastasis in experimental models, where tumor cellswere delivered directly into the blood stream (8). However, in order totranslate the results into clinical practice, such experimentalevaluations should be performed in syngeneic spontaneous models. Themurine mammary 4T1 cell line is a perfect model. In particular,sLe.^(x)-Neg variant is an appropriate model as it does not expressoverlapping selectin reactive epitopes sLe^(x/a).

BALB/c female mice (6-8 weeks old) were purchased from Harlan(Indianapolis, Ind.). Tumors were established as described earlier (9).Briefly, each mouse was inoculated subcutaneously in the abdominalmammary gland with 5×10⁴ 4 T1 cells. To establish a functionalcorrelation between P-Selectin ligand expression of 4T1 cells and theirmetastatic ability in vivo, we injected mice with 100 units of heparin30 minutes before tumor cell inoculation. Mice were sacrificed 26 daysafter tumor inoculation, lungs were harvested and metastatic cells weredetected by clonogenic assay. We observed a complete absence ofmetastases in lung of majority of mice (six mice out of total of seven)injected with heparin (Table 3). All mice that were injected with PBS ascontrol developed lung metastasis. Thus, blocking of P-Selectininteraction with its ligand in vivo significantly preventedestablishment of metastatic foci.

TABLE 3 Number of mice detected positive for established lung metastasesin groups administered with heparin or PBS. Total number of miceexamined in each experiment is given in the parenthesis. TreatmentPositive (total) PBS  6 (6) Heparin *1 (7) *P = 0.0047 as compared withPBS treated group by Fisher exact test.

Similarly, no mice were detected positive for lung metastases aftertreatment with Chondroitinase ABC (Table 4).

TABLE 4 Number of mice detected positive for established lung metastasesafter chonditinase ABC treatment of the cancer cells. Treatment Positive(total) ChABC *0 (5) Non-treated  5 (5) *P = 0.0079 as compared withgroup injected with non-treated cells by Fisher exact test.

Example 13

P-Selectin binds to CS PGs on the surface of human renal adenocarcinoma(10). To further explore the nature of P-Selectin ligands on the 4T1tumor cell line, used heparinase and chondroitinase ABC were usedseparately in P-Selectin binding assays. The data indicate a major rolefor CS in P-Selectin binding to the 4T1 cells (FIG. 12). FIG. 12Aillustrates 4T1 cells incubated with secondary antibody alone. FIG. 12Billustrates P-Selectin binding to 4T1 cells. FIG. 12C illustratesP-Selectin binding to 4T1 cells which had been pre-treated withheparinase. FIG. 12D illustrates P-Selectin binding to 4T1 cells whichhad been pre-treated with chondroitinase. FIG. 12E illustratesP-Selectin binding to 4T1 cells which had been pre-treated with bothheparinase and chondroitinase.

Example 14

Chondroitin sulfates, including chondroitin sulfates A, B, C and E,block the interaction of P-Selectin to cancer cells. Binding ofrecombinant P-Selectin to cells was examined after treatment withheparinase and chondroitinase ABC or in the presence of variousconcentrations of heparin and chondroitin sulfate A, B, C, and E(Seikagaku America, Falmouth, Mass.). Among those tested, CS B (dermatansulfate) and CS E inhibited P-Selectin binding to the cells (FIGS. 13and 14). CS A and C (data not shown) showed minimal inhibitory effects.CS B showed inhibitory effects only at higher concentrations, while CS Ewas a more potent inhibitor with a complete inhibition at aconcentration of 0.5 mg/ml. The effective dose of heparin, 120 units(FIG. 10), corresponds to 0.7 mg/ml heparin, which is close to the CS Eblocking concentration of 0.5 mg/ml. FIG. 13A illustrates 4T1 cellsincubated with secondary antibody alone. FIG. 13B illustrates P-Selectinbinding to 4T1 cells. FIG. 13C illustrates P-Selectin binding to 4T1cells when the P-Selectin had been pre-treated with 5.0 mg/mlchondroitin sulfate A. FIG. 13D illustrates P-Selectin binding to 4T1cells when the P-Selectin had been pre-treated with 5.0 mg/mlchondroitin sulfate B. FIG. 13E illustrates P-Selectin binding to 4T1cells when the P-Selectin had been pre-treated with 0.5 mg/mlchondroitin sulfate A. FIG. 13F illustrates P-Selectin binding to 4T1cells when the P-Selectin had been pre-treated with 0.5 mg/mlchondroitin sulfate B. FIG. 13G illustrates P-Selectin binding to 4T1cells when the P-Selectin had been pre-treated with 0.05 mg/mlchondroitin sulfate A. FIG. 13H illustrates P-Selectin binding to 4T1cells when the P-Selectin had been pre-treated with 0.05 mg/mlchondroitin sulfate B. FIG. 13I illustrates P-Selectin binding to 4T1cells when the P-Selectin had been pre-treated with 0.005 mg/mlchondroitin sulfate A. FIG. 13J illustrates P-Selectin binding to 4T1cells when the P-Selectin had been pre-treated with 0.005 mg/mlchondroitin sulfate B.

Example 15

FIG. 14A illustrates 4T1 cells incubated with secondary antibody alone.FIG. 14B illustrates P-Selectin binding to 4T1 cells. FIG. 14Cillustrates P-Selectin binding to 4T1 cells when the P-Selectin had beenpre-treated with 0.5 mg/ml chondroitin sulfate E. FIG. 14D illustratesP-Selectin binding to 4T1 cells when the P-Selectin had been pre-treatedwith 0.05 mg/ml chondroitin sulfate E. FIG. 14E illustrates P-Selectinbinding to 4T1 cells when the P-Selectin had been pre-treated with 0.005mg/ml chondroitin sulfate E. FIG. 14F illustrates P-Selectin binding to4T1 cells when the P-Selectin had been pre-treated with 0.0005 mg/mlchondroitin sulfate E. These data indicate that chondroitin sulfate isthe major P-Selectin ligand on the surface of the 4T1 cells.Oversulfated CS E is able to effectively inhibit the interactions.

Example 16

The bone-colonizing human breast cancer cell variant MDA-MET was testedfor expression of P-Selectin ligands. P-Selectin reactivity with cellswas decreased after chondroitinase treatment (FIG. 15). Heparinase or amixture of heparinase and chondroitinase did not affect P-Selectinbinding. This data suggests that CS PGs can also be a major P-Selectinligand on the surface of human breast cancer cells. FIG. 15A illustratesMDA-MET cells incubated with secondary antibody alone. FIG. 15Billustrates P-Selectin binding to MDA-MET cells. FIG. 15C illustratesP-Selectin binding to MDA-MET cells when the cells had been pre-treatedwith heparinase. FIG. 15D illustrates P-Selectin binding to MDA-METcells when the cells had been pre-treated with chondroitinase. FIG. 15Eillustrates P-Selectin binding to MDA-MET cells when the cells had beenpre-treated with both heparinase and chondroitinase. FIG. 15Fillustrates P-Selectin binding to MDA-MET cells when the P-Selectin hadbeen pre-treated with 10.0 mg/ml of a chondroitin sulfate andglycosaminoglycan mixture. FIG. 15G illustrates P-Selectin binding toMDA-MET cells when the P-Selectin had been pre-treated with 1.0 mg/ml ofa chondroitin sulfate and glycosaminoglycan mixture.

Example 17

Real-time PCR was conducted to quantify mRNAs of five genes in fourdifferent human breast cancer tumor lines. The assayed genes wereSyndecan-1 (SDC-1), Neuropilin-1 (NRP-1), Syndecan-4 (SDC-4), MCSP, andestrogen receptor 1. The tumor lines were MCF7, MDA-MD-468 (MDA-468),MDA-MB-231 (MDA-231), and MDA-MET. MCF-7 and MDA-468 are lessaggressive. MDA-231 is an aggressive cell line, and MDA-MET is a sublineof MDA-231 that metastasizes to bone. The quantity of each mRNA wasassayed in comparison to 18s RNA. The results are shown in Table 5.NRP-1, SDC-4 and MCSP expression was higher in the two more aggressivecell lines than in either of the two less aggressive cell lines. Theresults suggest a down regulation of SDC-1 and an up regulation of SDC-4is related to the more aggressive phenotype. MCF-7 and MDA-468 areepithelial-like, while both MDA-231 and MDA-MET cells are mesenchymaltype. Thus, high expression of NRP-1, MCSP and SDC-4 may be related toan epithelial to mesenchymal transition, which is a phenotypic eventassociated with more metastasis and aggressive growth.

TABLE 5 Ratio of mRNA for indicated genes to 18s RNA. Antigen MCF7MDA-231 MDA-231 MDA-MET SDC-1 0.37 2.3 0.26 0.17 NRP-1 0.84 0.91 1.321.99 SDC-4 0.67 0.83 1.2 2.01 MCSP 0.01 0.02 3.14 1.53 Estrogen receptor1 5.13 0.13 0.15 0.11

Example 18

Cell lysates of MDA-231 tumor cells were probed by Western blotting toidentify NRP-1 protein and the proteins that bind P-Selectin. Theresults are shown in FIG. 16. In FIG. 16, panel A, lane 1, an MDA-231cell lysate is probed with recombinant P-Selectin, and in lane 2 withanti-Neuropilin-1, and in lane 3 with anti-CS-A. The long arrowindicates the NRP-1 core protein. The short arrows indicate NRP-1 with asulfated glycosaminoglycan (GAG) chain. Panel B shows a Western blot ofproteins that were immunoprecipitated by P-Selectin (attached to ProteinG beads (DYNA BEADS system)). The gel in panel B was probed withanti-NRP-1. These data indicate that Neuropilin-1 is decorated with CSand is one of the primary proteins of MDA-231 cell lysate that is boundby P-Selectin, and that only the CS-decorated form of Neuropilin-1 bindsto P-Selectin.

Example 19

Analogously to Example 18, MDA-231 cell lysate was analyzed by Westernblotting with anti-Syndecan-4 and human P-Selectin. The results areshown in FIG. 17. Lanes 1, 2, and 4 are total cell lysates of MDA-231.Lane 3 is proteins immunoprecipitated with P-Selectin, as in Example 18.Lanes 1, 3, and 4 were probed with polyclonal anti-Syndecan-4antibodies. Lane 2 is probed with P-Selectin. Arrows show bands thatcorrespond to Syndecan-4 and react with P-Selectin. These data show thatSyndecan-4 binds to P-Selectin.

Example 20

The melanoma cell line M14 does not express MCSP. M14 and M14 cellstransfected with a vector to express MCSP were analyzed by fluorescenceactivated cell sorting (FACS) with antibodies against CS-A (2H6),antibodies against MCSP (225.28) and P-Selectin coupled to human Fcchain in FIG. 18. The cells labeled with primary antibody or P-Selectinwere then reacted with secondary fluorescently labeled anti-Fc antibodyand sorted. The leftmost panels of FIG. 18 are control M14 cells labeledonly with secondary antibody. The middle panels labeled M14 areuntransformed M14 cells labeled with the primary antibody or P-Selectinshown on the left. The right most panels are M14-MCSP cells. The resultssuggest that binding of P-Selectin to the tumor cells is via MCSP.

Example 21

As in Example 17, real-time PCR was used to quantify mRNA of severalenzymes involved in CS biosynthesis. The results are shown in FIG. 19.The tested mRNAs were for C4ST-1 (also known as CHST11), whichsynthesizes CS-A, GalNAc4S-6ST, which synthesizes CS-E, CHST3, whichsynthesizes CS-C, and SART2, which is dermatin sulfate epimerase andconverts CS-A to CS-B. The data show CHST11 mRNA is highest in MDA-231and MDA-MET cells, the more aggressive of the four tumor cell linestested, and lower in the less aggressive lines MCF7 and MDA-468. Theother genes assayed were also highly expressed in most or all of thetumor lines, but were not more highly expressed in the two aggressivetumor lines than in the two less aggressive tumor lines.

Example 22

In this experiment, gene expression levels were assayed by real-time PCRand comparison to 18S RNA levels. The dependence of gene expression onmethylation levels was tested by treating tumor cells with varyinglevels of 5-aza-2′-deoxycytidine (5azadC), which is a demethylatingagent (Table 6). Methylation of CpG islands is a well-known mechanism ofgene control. Methylation decreases expression of genes whose promotersare methylated. The expression of NRP-1, CHST11, and MCPG each increasedwith increasing 5azadC concentration, which indicates they are undermethylation control, with increased methylation repressing expression ofthe genes. Urokinase (uPA) was used as a positive control. Syndecan-4expression decreased or remained approximately constant with 5azadCtreatment, indicating it is not under methylation control.

TABLE 6 Expression of indicated genes in MCF-7 cells after treatmentwith 5azadC. Relative expression levels are shown compared with no (0μm) 5azadC. 5azadC (μM) NRP-1 CHST11 MCPG uPA Synd-4 0 1 1 1 1 1 0.51.04 1.34 1.3 2.2 0.7 1 1.50 1.68 1.4 2.9 0.5 5 1.72 3.7 1.7 3.2 0.8 201.71 4.00 2.1 3.9 0.6

Example 23

This Example demonstrates that administration of CS reduces metastasis.Mice were injected with 4T1 cells into fat pads. After tumors werepalpable (3-4 days after transplant) the mice were daily injected withCS intraperitoneally (ip) or subcutaneously (sc). The mice weresacrificed 30 days after transplant and lung colonies were quantified.CS was dissolved in saline for injection. Saline control injection byeither sc or ip routes produced similar results. Injection of either 1mg or 10 mg CS subcutaneously decreased metastasis compared to salinecontrol, but injection intraperitoneally did not appear to (FIG. 20).

Characterization of P- and E-Selectin ligands is important for theassessment of metastatic risk and the development of possible ways ofdealing with metastatic disease. A significant amount of P-Selectinbinding is both Ca²⁺-independent and sialic acid-independent, confirmingthat sLe^(x) is not a P-Selectin ligand on 4T1 cells.

While sLe^(x/a) oligosaccharides are common ligands for both E- andP-Selectin, these two lectins do not correlate in their reactivity withthe 4T1 cells. P-Selectin binds to the 4T1 cells strongly and thebinding is not affected by sorting for sLe^(x) oligosaccharide by KM93antibody or even by FTIII gene transfection. E-Selectin binding can bepredicted by reactivity of anti-sLe^(x) antibodies, indicating thatE-Selectin binding is predominately sLe^(x) dependent. However,P-Selectin binding did not correlate with either E-Selectin orsLe^(x)-reactive antibodies, suggesting that much of the P-Selectinbinding is not to sLe^(x) or other related oligosaccharides. There is acorrelation between sLe^(x) reactive antibody binding and E-Selectinbinding to tumor cells but no such correlation to P-Selectin binding.The P-Selectin binding in 4T1 is dependent upon structures other thansLe^(x) or sLe^(a) ligands with increased sLe^(x) expression havingalmost no effect on P-Selectin binding.

E-Selectin binding to the 4T1 cell line is restricted to sLe^(x) orclosely related structures while P-Selectin binding can involve a variedgroup of compounds, including Ca²⁺-independent binding to non-Lewisstructures. Characterization of P-Selectin binding to the 4T1 cellsillustrates that this interaction is sulfur dependent andheparinase/chondroitinase sensitive. Further characterization of the 4T1surface ligands clearly indicate that CS and CS glycosaminoglycans arethe major P-Selectin ligands expressed on this cell line. CS B and CS Eare able to inhibit the interaction.

The stable expression of P-Selectin ligands on 4T1 cells in vivosuggests that these ligands contribute to the metastatic behavior ofthis cell line. Cell surface P-Selectin ligands indeed contribute tobinding of the 4T1 cells to platelets and HUVECs. Intact P-Selectinreactivity with heparan sulfate or CS may facilitate microemboliformation and adhesion to the endothelial cells, promoting tumor cellarrest in vasculature and extravasation.

Heparin is being used as anticoagulant treatment of venousthromboembolism in cancer patients, where it has been shown to improvepatient survival by mechanisms not explained by anticoagulation (11).The present invention clearly demonstrates that Heparin inhibitedP-Selectin binding to the 4T1 cells, and it blocked P-Selectin mediatedadhesion of platelets to this tumor cell line. This data warranted invivo testing of heparin for inhibition of metastasis in tumor bearinganimals.

Inhibition of interaction between P-Selectin with its various ligands ontumor cells has an anti-metastatic therapeutic effect. Competitionstudies demonstrate that heparin and CS interaction may involve a regionof the P-Selectin molecule very close to the lectin binding site forsLe^(x). Heparin is capable of blocking P-Selectin binding to varioustumor cells with various surface ligands, including sLe^(x) (12),sulfated glycolipids (13), heparan sulfate PGs (14, 15) and even CS PGs(10). In addition, the binding of a CS proteoglycan to P-Selectin wasinhibited by sLe^(x), which is in agreement with the notion that CSbinding to the lectin domain of P-Selectin is similar to sLe^(x) binding(10). The present data suggest that highly sulfated CS types may be usedto block P-Selectin binding to any of its ligands on tumor cells. Suchbroad specificity can be explained by recognition of a clustered epitopeby P-Selectin (6). Targeting P-Selectin interaction with these ligandscan be used for treatment of metastatic cancer. The current data supportadministration of CS as an alternative to treat metastatic disease.

As various changes could be made in the above methods and compositionswithout departing from the scope of the invention, it is intended thatall matter contained in the above description be interpreted asillustrative and not in a limiting sense. Unless explicitly stated torecite activities that have been done (i.e., using the past tense),illustrations and examples are not intended to be a representation thatgiven embodiments of this invention have, or have not, been performed.

As various changes could be made in the above methods and compositionswithout departing from the scope of the invention, it is intended thatall matter contained in the above description be interpreted asillustrative and not in a limiting sense. Unless explicitly stated torecite activities that have been done (i.e., using the past tense),illustrations and examples are not intended to be a representation thatgiven embodiments of this invention have, or have not, been performed.

REFERENCES

-   1. Fukushi, Y., Nudelman, E., Levery, S. B., Hakomori, S., and    Rauvala, H. Novel fucolipids accumulating in human    adenocarcinoma. III. A hybridoma antibody (FH6) defining a human    cancer-associated difucoganglioside (VI3NeuAcV3III3Fuc2nLc6). J Biol    Chem, 259: 10511-10517, 1984.-   2. Fukushima, K., Hirota, M., Terasaki, P. I., Wakisaka, A.,    Togashi, H., Chia, D., Suyama, N., Fukushi, Y., Nudelman, E., and    Hakomori, S. Characterization of sialosylated Lewisx as a new    tumor-associated antigen. Cancer Res, 44: 5279-5285, 1984.-   3. Hanai, N., Shitara, K., and Yoshida, H. Generation of monoclonal    antibodies against human lung squamous cell carcinoma and    adenocarcinoma using mice rendered tolerant to normal human lung.    Cancer Res, 46: 4438-4443, 1986.-   4. Hoff, S. D., Matsushita, Y., Ota, D. M., Cleary, K. R., Yamori,    T., Hakomori, S., and Irimura, T. Increased expression of    sialyl-dimeric LeX antigen in liver metastases of human colorectal    carcinoma. Cancer Res, 49: 6883-6888, 1989.-   5. Dohi, T., Nemoto, T., Ohta, S., Shitara, K., Hanai, N., Nudelman,    E., Hakomori, S., and Oshima, M. Different binding properties of    three monoclonal antibodies to sialyl Le(x) glycolipids in a gastric    cancer cell line and normal stomach tissue. Anticancer Res, Vol. 13,    pp. 1277-1282, 1993.-   6. Koenig, A., Norgard-Sumnicht, K., Linhardt, R., and Varki, A.    Differential interactions of heparin and heparan sulfate    glycosaminoglycans with the selecting. Implications for the use of    unfractionated and low molecular weight heparins as therapeutic    agents. J Clin Invest, 101: 877-889, 1998.-   7. Kawashima, H., Atarashi, K., Hirose, M., Hirose, J., Yamada, S.,    Sugahara, K., and Miyasaka, M. Oversulfated chondroitin/dermatan    sulfates containing GlcAbeta1/IdoAalpha1-3GalNAc(4,6-O-disulfate)    interact with L- and P-Selectin and chemokines. J Biol Chem, 277:    12921-12930, 2002.-   8. Stevenson, J. L., Choi, S. H., and Varki, A. Differential    metastasis inhibition by clinically relevant levels of    heparins—correlation with selectin inhibition, not antithrombotic    activity. Clin Cancer Res, 11: 7003-7011, 2005.-   9. Monzavi-Karbassi, B., Artaud, C., Jousheghany, F., Hennings, L.,    Carcel-Trullols, J., Shaaf, S., Korourian, S., and Kieber-Emmons, T.    Reduction of Spontaneous Metastases through Induction of    Carbohydrate Cross-Reactive Apoptotic Antibodies. J Immunol, 174:    7057-7065, 2005.-   10. Kawashima, H., Hirose, M., Hirose, J., Nagakubo, D., Plaas, A.    H., and Miyasaka, M. Binding of a large chondroitin sulfate/dermatan    sulfate proteoglycan, versican, to L-Selectin, P-Selectin, and CD44.    J Biol Chem, 275: 35448-35456, 2000.-   11. Cosgrove, R. H., Zacharski, L. R., Racine, E., and    Andersen, J. C. Improved cancer mortality with low-molecular-weight    heparin treatment: a review of the evidence. Semin Thromb Hemost,    28: 79-87, 2002.-   12. Nelson, R. M., Cecconi, O., Roberts, W. G., Aruffo, A.,    Linhardt, R. J., and Bevilacqua, M. P. Heparin oligosaccharides bind    L- and P-Selectin and inhibit acute inflammation. Blood, 82:    3253-3258, 1993.-   13. Borsig, L., Wong, R., Hynes, R. O., Varki, N. M., and Varki, A.    Synergistic effects of L- and P-Selectin in facilitating tumor    metastasis can involve non-mucin ligands and implicate leukocytes as    enhancers of metastasis. Proc Natl Acad Sci USA, 99: 2193-2198,    2002.-   14. Wei, M., Tai, G., Gao, Y., Li, N., Huang, B., Zhou, Y., Hao, S.,    and Zeng, X. Modified heparin inhibits P-Selectin-mediated cell    adhesion of human colon carcinoma cells to immobilized platelets    under dynamic flow conditions. J Biol Chem, 279: 29202-29210, 2004.-   15. Ma, Y. Q. and Geng, J. G. Heparan sulfate-like proteoglycans    mediate adhesion of human malignant melanoma A375 cells to    P-Selectin under flow. J Immunol, 165: 558-565, 2000.-   16. Nazaruk R A, Rochford R, Hobbs M V, Cannon M J. Functional    diversity of the CD8+ T cell response to Epstein-Barr virus:    Implications for the pathogenesis of EBV-associated    lymphoproliferative disorders. Blood 1998; 91:3875-83.-   17. Miller, V. M. et al. 2004, Nucleic Acids Res. 32:661-668.-   18. McManus, M T et al., 2002, Nature Rev. Genet. 3:737-747.-   19. Miller, V M et al., 2003, Proc. Natl. Acad. Sci. USA    100:7195-7200.-   20. U.S. Published Patent Application No. 20060154370.-   21. Kitagawa, H et al. 2003, J. Biol. Chem. 278:23666-23671.-   22. Sugahara, K et al., 2003, Current Opinion in Structural Biology    13:612-620.

All references cited in this specification are hereby incorporated byreference in their entirety. The discussion of the references herein isintended merely to summarize the assertions made by their authors and noadmission is made that any reference constitutes prior art relevant topatentability. Applicant reserves the right to challenge the accuracyand pertinence of the cited references.

What is claimed is:
 1. A method of treating breast cancer comprising:administering to a patient an antibody against Melanoma ChondroitinSulfate Proteoglycan (MCSP), wherein the antibody specificallyrecognizes MCSP in its form with chondroitin sulfate (CS) attached toMCSP and does not bind to MCSP in its form without CS attached to MCSPand reduces interaction between P-selectin and cells expressing MCSP andcomprising chondroitin sulfate (CS).
 2. A method of inhibitingmetastasis in a mammal afflicted with cancer or suspected to beafflicted with cancer comprising: administering to the mammal anantibody against Melanoma Chondroitin Sulfate Proteoglycan (MCSP),Syndecan-1, Syndecan-4, or Neuropilin-1, wherein the antibodyspecifically recognizes MCSP, Syndecan-1, Syndecan-4 or Neuropilin-1 intheir forms with chondroitin sulfate (CS) attached to the MCSP,Syndecan-1, Syndecan-4 or Neuropilin-1, and does not bind to MCSP,Syndecan-1, Syndecan-4, or Neuropilin-1 in their forms without CSattached to the MCSP, Syndecan-1, Syndecan-4, or Neuropilin-1, andreduces interaction between P-selectin and cells expressing MCSP,Syndecan-1, Syndecan-4, or Neuropilin-1, and comprising chondroitinsulfate (CS).
 3. The method of claim 2 wherein the antibody specificallyrecognizes MCSP in its form with CS attached to the MCSP and does notbind to MCSP in its form without CS attached to the MCSP.
 4. The methodof claim 2 wherein the antibody specifically recognizes Syndecan-1 inits form with CS attached to the Syndecan-1 and does not bind toSyndecan-1 in its form without CS attached to the Syndecan-1.
 5. Themethod of claim 2 wherein the antibody specifically recognizesSyndecan-4 in its form with CS attached to the Syndecan-4 and does notbind to Syndecan-4 in its form without CS attached to the Syndecan-4. 6.The method of claim 2 wherein the antibody specifically recognizesNeuropilin-1 in its form with CS attached to the Neuropilin-1 and doesnot bind to Neuropilin-1 in its form without CS attached toNeuropilin-1.